51st week of 2012 patent applcation highlights part 56 |
Patent application number | Title | Published |
20120323200 | COOLING COMPOSITION AND ABSORBENT ARTICLE COMPRISING THE SAME - A cooling composition comprising a cooling agent together with a polyethylene glycol (PEG) or a mixture of different PEGs having high molecular weights and an absorbent article comprising the cooling composition. The cooling agent of the composition has a reduced tendency to vaporize and evaporate at room temperature. | 2012-12-20 |
20120323201 | ABSORBENT ARTICLE INCLUDING AN ABSORBENT CORE LAYER HAVING A MATERIAL FREE ZONE AND A TRANSFER LAYER ARRANGED BELOW THE ABSORBENT CORE LAYER - An absorbent article including a liquid permeable cover layer, a liquid impermeable barrier layer, an absorbent core arranged adjacent to the cover layer, the absorbent core including a material-free zone extending, a transfer layer arranged between the core and the barrier layer, the transfer layer including a planar portion having an upper surface and a lower surface and a protrusion extending upwardly from the upper surface. | 2012-12-20 |
20120323202 | ABSORBENT ARTICLE INCLUDING AN ABSORBENT CORE LAYER HAVING A MATERIAL FREE ZONE AND A TRANSFER LAYER ARRANGED BELOW THE ABSORBENT CORE LAYER - An absorbent article including a liquid permeable cover layer, a liquid impermeable barrier layer, an absorbent core arranged adjacent to the cover layer, the absorbent core including a material-free zone extending, a transfer layer arranged between the core and the barrier layer, the transfer layer including a planar portion having an upper surface and a lower surface and a protrusion extending upwardly from the upper surface. | 2012-12-20 |
20120323203 | METHOD FOR MAKING PACKAGE-ABSORBENT ARTICLE ASSEMBLY AND PACKAGE-ABSORBENT ARTICLE ASSEMBLY OBTAINED BY THE SAME - A method for packaging an absorbent article assembly that includes following the steps. First and second breast milk absorbent pads are fed onto wrapping sheet web. Next, the first breast milk absorbent pad is displaced from a transverse center line toward an upper end by ¼ of a dimension thereof as measured in a longitudinal direction, and the second breast milk absorbent pad is displaced from a transverse center line toward an lower end by ¼ of a dimension thereof as measured in a longitudinal direction. Next, the first and second breast milk absorbent pads are folded back from the upper and lower ends toward the transverse center line. Next, the upper and lower ends of the wrapping sheet web are folded back toward the transverse center line. Next, a joint zone is formed between the first and second breast milk absorbent pads and the pads are cut apart. | 2012-12-20 |
20120323204 | DISPOSABLE ABSORBENT GARMENT HAVING COLORED FACINGS AND INTEGRAL WAISTBAND - A garment comprises a laminate. The laminate comprises a first layer colored a first color, and a second layer colored a second color different than the first color. The laminate includes a folded flap in the waist region, thereby defining an integral, outwardly visible waistband having a waistband lower edge. In one embodiment, the first layer and the second layer are coterminous at the waistband lower edge. In particular embodiments, the folded flap is an outwardly folded flap, and the first layer is an inner layer and the second layer is an outer layer, and the outwardly visible waistband is colored the first color. The distinction between the first color and second color in conjunction with the fold creates a visible waistband effect. | 2012-12-20 |
20120323205 | Burn diaper - An embodiment includes a sterile package containing a disposable diaper with a dressing attached to the inner surface of the diaper. The dressing is impregnated with an antibiotic or other therapeutic ointment containing bacitracin. Embodiments are used as dressings for pediatric burn patients. Embodiments allow the replacement of dressings in such patients by a single care-giver. Other embodiments are used with adult patients with wounds in the pelvic area. | 2012-12-20 |
20120323206 | BARRIER FLAP FOR AN ABSORBENT ARTICLE - An elastic barrier flap for an absorbent article includes a web configured to define a gap and a plurality of elastic members captured by the web. The plurality of elastic members is symmetrically arranged about the gap defined by the web. The web and plurality of elastic members are adapted to inhibit the transverse flow of body exudates released by a wearer of the absorbent article. | 2012-12-20 |
20120323207 | ABSORBENT ARTICLE - An absorbent article | 2012-12-20 |
20120323208 | Medication Dose Preparation and Transfer System - Apparatus, systems, methods and articles are described to prepare and track medications and medication containers as they are prepared, administered to patients and, in some cases, disposed of. Information such as medication type, concentration, and volume are associated with medication containers during preparation and this information can later be consumed/utilized when administering the medication from a container to a patient. Disposing of any remaining medication can also be tracked. | 2012-12-20 |
20120323209 | CONTAINER, SYSTEM AND METHOD FOR PROVIDING A SOLUTION - A container ( | 2012-12-20 |
20120323210 | FLUID TRANSFER ASSEMBLY WITH VENTING ARRANGEMENT - A fluid transfer assembly including a vented female vial adapter and male vial adapter for use with a pair of vials including a vial with contents under negative pressure for liquid drug reconstitution and administration purposes. The vented female vial adapter includes a venting arrangement and the male vial adapter includes a sealing arrangement for selectively sealing the venting arrangement. The fluid transfer assembly is designed such that only filtered air is drawn into the vial under negative pressure subsequent to reconstitution of liquid drug contents to ensure sterile conditions. | 2012-12-20 |
20120323211 | Coated Balloons for Blood Vessel Stabilization - A coated balloon device for stabilizing a section of a blood vessel in a living subject is disclosed. The coating layer of the coated balloon comprises a phenolic compound having a plurality of phenolic groups connected to form a hydrophobic core with peripheral phenolic hydroxyl groups. The coating layer of the coated balloon may contain a hydrophilic polymer to facilitate the release of the phenolic compound. The balloon in general is made of a compliant polymer for atraumatic contact with the blood vessel. In some embodiments, the coating of the coated balloon device further comprises a hydrophilic undercoat layer between the balloon and the coating layer. In some embodiments, the coated balloon device further comprises a sacrificial top coating that dissolves upon delivery into the section of the blood vessel and comprises a hydrophilic composition including sugar, sugar derivatives, or a combination thereof. | 2012-12-20 |
20120323212 | DISTRIBUTED MEDICATION DELIVERY SYSTEM AND METHOD HAVING AUTONOMOUS DELIVERY DEVICES - A pump operations module having a base function includes only base function programming in the module itself but is configured to receive advanced delivery programs in a buffer for execution autonomously. An advanced interface module (AIM) is used to prepare advanced delivery programs and upload them to one or more delivery modules as well as monitor the performance of those modules. However, the advanced interface module does not control the execution of those advanced delivery programs by the pump operations modules. The AIM includes a touch screen and access to drug libraries. The AIM will generate graphical slide controls on the touch screen with the minimum and maximum values on the touch screen for the user to create an advanced delivery program for upload, to greatly lessen the risk of errors. Support for PK applications is provided. | 2012-12-20 |
20120323213 | THERMO-CHEMICAL MEDICAL DEVICE FOR MANIPULATION OF TISSUE - The present invention provides a medical device for manipulation of tissue of a patient. The medical device comprises a shaft having a proximal section extending to a distal section that has a closed distal end portion. The shaft has a plurality of lumens formed therein including a first lumen and a second lumen. The first lumen is for distally advancing a first reactant through the proximal section. The second lumen is for distally advancing a second reactant through the proximal section. Positioned longitudinally within the shaft and distally from the first and second lumens is a mixing element. The mixing element is in fluid communication with the first and second lumens. The mixing element has a series of baffles for mixing the first and second reactants together producing a reaction product to heat the closed distal end portion of the shaft for manipulation of the tissue. | 2012-12-20 |
20120323214 | ALZHEIMER'S DISEASE TREATMENT WITH MULTIPLE THERAPEUTIC AGENTS DELIVERED TO THE OLFACTORY REGION THROUGH A SPECIAL DELIVERY CATHETER AND IONTOPHORESIS - This invention describes the administration of multiple therapeutic agents with insulin in conjunction with bexarotene, ketamine, monoclonal antibodies Etanercept, IGF-1, and acetylcholine esterase inhibitors physostigmine, for treatment of Alzheimer's disease and other neurodegenerative diseases. Insulin, improves memory; also augments and amplifies the effects of the adjuvant therapeutic agents (paracrine and intracrine effects) and consequently reduces the β amyloid, its soluble precursors, prevents damage to the neuronal skeletal network (taupathy), and blocks glutamate excitotoxicity, reduces brain inflammation, prevents apoptosis, and increases the acetylcholine levels in the neurons and synapses; by using a combination of insulin, bexarotene, ketamine, Etanercept, IGF-1, and physostigmine therapeutic agents. The results are achieved by using the specially designed Iontophoresis incorporated olfactory mucosal delivery (ORE) catheter device located at the olfactory nerves, sphenoid sinus, and adjacent structures described here, to transport the large molecules of therapeutic agents to treat AD delivered to the CNS bypassing BBB from ORE. | 2012-12-20 |
20120323215 | System and method for administering medicaments on the basis of urine values - The invention relates to a system and a method for administering medicaments to a patient, comprising: at least a first measuring device ( | 2012-12-20 |
20120323216 | NEEDLESHIELD ASSEMBLY - A needleshield assembly including a needle hub, hypodermic needle and protective cover is disclosed in which the protective cover can both secure and disable the needle following use. | 2012-12-20 |
20120323217 | Cranial Evacuation System and Use Thereof - The present invention relates to a method and device for removing solid matter from a brain and controlling bleeding associated with the removal of the matter. The method involves securing a cranial anchor to a region of the skull in which an opening has been created to expose brain matter and introducing through a passage defined by the anchor a channel member that displaces brain tissue and exposes the solid matter. After removing the solid matter, a flowable hemostat is introduced into the cavity created by removal of the matter. A balloon introduced into the working channel is then inflated to compress the hemostat against the wall of the cavity to control bleeding from blood vessels around the cavity. The device includes a cranial anchor, a channel member defining a working channel, an optional removable trocar, and a catheter for introducing the hemostat and the inflatable balloon into the cavity. | 2012-12-20 |
20120323218 | DRUG-DELIVERY PUMPS AND METHODS OF MANUFACTURE - Embodiments of an implantable electrolytic pump include an electrolysis chamber, a drug chamber and an osmosis chamber, the osmosis chamber having a first portion in contact with the drug chamber and a second portion exposed to facilitate contact with a surrounding fluid. The pump further includes a cannula for conducting liquid from the drug chamber and electrolysis electrodes within the electrolysis chamber for causing generation of a gas therein, the electrolysis and drug chambers being in contact such that gas electrolysis within electrolysis chamber forces fluid from the drug chamber into the cannula, contact between the drug chamber and the osmosis chamber permitting fluid admitted into the osmotic chamber from the surrounding fluid to offset volume loss from the drug chamber and prevent buildup of vacuum pressure thereon. | 2012-12-20 |
20120323219 | DELIVERING DRUGS TO DESIRED LOCATIONS WITHIN A MAMMAL - This document provides materials and methods related to delivering drugs to desired locations within a mammal. For example, materials and methods for implanting a guide wire and a drug eluting implant into a mammal are provided. | 2012-12-20 |
20120323220 | ENDOLUMINAL DRUG DELIVERY DEVICES AND METHODS - A device and method for delivering a drug from inside a body lumen to tissue surrounding the body lumen. An endoluminal drug delivery device includes a dual-lumen catheter for housing a guidewire and a needle connectable to a drug source. The guidewire exits the catheter through an opening at the distal end, and the needle exits the catheter through an exit port in the outer wall of the catheter. A distal portion of the catheter has a single lumen and includes a taper, allowing the distal tip to act as a dilator. The device optionally includes a catheter lumen splitter and/or a handpiece assembly. A method of delivering fluid to tissue surrounding a body lumen includes inserting a guidewire into the body lumen, tracking the device over the guidewire, deploying the needle through the exit port to the tissue, delivering fluid, and retracting the needle into the catheter. | 2012-12-20 |
20120323221 | Adapter Cap and Nasal Washing System Using the Cap - An adapter cap is configured to convert a plastic water or drinking bottle into a nasal washing device. The cap has a connector portion or mechanism configured for engagement with the neck of a plastic water bottle in place of a conventional bottle cap, and a tapered applicator or spout portion having a tip with an opening which is configured for placing into a nostril of a user during a nasal washing procedure. | 2012-12-20 |
20120323222 | DEVICE AND METHOD FOR RAPID ASPIRATION AND COLLECTION OF BODY TISSUE FROM WITHIN AN ENCLOSED BODY SPACE - Device and method for rapid extraction of body tissue from an enclosed body cavity. Hollow entry cannula with optional core element provides entry into body tissue space such as bone marrow. Aspiration cannula is inserted through cannula into body tissue and is manipulated to advance directionally through body cavity. Optional stylet within aspiration cannula aids in advancing aspiration cannula through body tissue and is removed to facilitate extraction of body tissue through the aspiration cannula. Inlet openings near distal tip of aspiration cannula allow tissue aspiration, with negative pressure source at proximal end of aspiration cannula providing controlled negative pressure. Aspiration cannula may be withdrawn and its path adjusted for multiple entries through the same entry point, following different paths through tissue space for subsequent aspiration of more tissue. | 2012-12-20 |
20120323223 | APPLYING SHEAR STRESS FOR DISEASE TREATMENT - A system for applying shear stress ex-situ to a fluid. A method of preparing a fluid for intravenous administration to a patient. In some embodiments, the system comprises a shear device; and at least one device configured for intravenous administration of the fluid to a patient, the devices defining a fluid passage configured to be sterilized and maintained sterile during use, the fluid comprising at least one therapeutic fluid, blood, or a combination thereof. The shear device of the system is in fluid communication with the at least one device configured for intravenous administration of the fluid to a patient. | 2012-12-20 |
20120323224 | SELECTIVE CYTOPHERESIS DEVICES AND RELATED METHODS THEREOF - The present invention relates to systems and devices to treat and/or prevent inflammatory conditions within a subject and to related methods. More particularly, the invention relates to systems, devices, and related methods that sequester leukocytes and/or platelets and then inhibit their inflammatory action. | 2012-12-20 |
20120323225 | INTERNAL DEVICE FOR INJECTION AND SAMPLING OF A LIQUID INSIDE A LIVING ORGANISM - The invention concerns a device to inject and/or to take a sample, with the aid of a needle, of a liquid inside the organism of a living being, through the skin in a repeated manner. | 2012-12-20 |
20120323226 | QUICK CONNECT ASSEMBLY FOR USE BETWEEN SURGICAL HANDLE ASSEMBLY AND SURGICAL ACCESSORIES - A hand-held electromechanical surgical device is provided and configured to selectively connect with a surgical accessory. The surgical device includes a device housing defining a connecting portion for selectively receiving a coupling assembly of the surgical accessory. The connecting portion includes an annular wall defining a cylindrical recess dimensioned to receive the coupling assembly of the surgical accessory; a collar slidably supported about the annular wall, wherein the collar is slidable between a first position and a second position; and at least one socket member interposed between the annular wall and the collar, wherein each socket member is slidably supported in the annular wall. Each socket member includes a first fixed state wherein each socket member projects into the cylindrical recess of the annular wall; and a second movable state wherein each socket member is free to not project into the cylindrical recess of the annular wall. | 2012-12-20 |
20120323227 | METHODS AND DEVICES TO TREAT NASAL AIRWAYS - Methods and devices for treating nasal airways are provided. Such devices and methods may improve airflow through an internal and/or external nasal valve, and comprise the use of mechanical re-shaping, energy application and other treatments to modify the shape, structure, and/or air flow characteristics of an internal nasal valve, an external nasal valve or other nasal airways. | 2012-12-20 |
20120323228 | Laser coagulation of an eye structure from a remote location - An integral laser imaging and coagulation apparatus, and associated systems and methods that allow an ophthalmologist to perform laser retinal surgical procedures with an integral laser imaging and coagulation apparatus disposed at a first (i.e. local) location from a control system disposed at a second (i.e. remote) location, e.g., a physician's office. In some embodiments, communication between the integral laser imaging and coagulation apparatus and control system is achieved via the Internet®. | 2012-12-20 |
20120323229 | EYE-SAFE DEVICE FOR TREATMENT OF SKIN TISSUE - Methods and devices are described that provide for eye-safe treatments using a photocosmetic device on skin tissue. In particular, various eye-safety devices protect the eye, including both the retina and the iris, as well as provide additional skin safety. The devices and methods described are particularly useful in consumer devices, but are useful in other devices also. | 2012-12-20 |
20120323230 | LASER FUSION OF TISSUE LAYERS - A laser tissue fusion device is optimized for particular surgical applications to join tissue layers. The device has two opposed arms that engage and disengage to clamp and release layers of tissue therebetween. The distal end of the first arm is disposed opposite the distal end of the second arm. A laser energy source generates therapeutic laser energy is either integrated within the device is a separate unit. An energy pathway transmits the laser energy to the distal end of the first arm to deliver the laser energy to tissue layers clamped between the distal ends of the arms. An actuator decreases the separation distance between the distal ends of the arms to clamp the tissue layers. A switch activates the laser energy source upon engagement. The laser energy source delivers a burst of energy at a predetermined wavelength for a predetermined period of time sufficient to spot-weld the tissue. | 2012-12-20 |
20120323231 | ELECTROSURGICAL INSTRUMENT - An electrosurgical instrument includes an instrument shaft having a longitudinal axis, and an electrode assembly at one end of the shaft, the electrode assembly including first, second and third electrodes which are electrically insulated one from another by means of one or more insulation members. The instrument further includes first and second connections by which RF energy can be supplied to the instrument from an electrosurgical generator. The first electrode is movable longitudinally between an advanced position in which it extends from the instrument shaft and a retracted position in which it is less advanced with respect to the instrument shaft. When the first electrode is in its advanced position, the first and second connections are in electrical communication with the first and second electrodes. When moved to its retracted position, the first and second connections are caused to be in electrical communication with the second and third electrodes. | 2012-12-20 |
20120323232 | METHODS AND DEVICES TO TREAT NASAL AIRWAYS - Methods and devices for treating nasal airways are provided. Such devices and methods may improve airflow through an internal and/or external nasal valve, and comprise the use of mechanical re-shaping, energy application and other treatments to modify the shape, structure, and/or air flow characteristics of an internal nasal valve, an external nasal valve or other nasal airways. | 2012-12-20 |
20120323233 | Renovascular treatment device, system, and method for radiosurgically alleviating hypertension - A radiosurgical method for treating cardiorenal disease of a patient, the method including directing radiosurgery radiation from outside the patient towards one or more target treatment regions encompassing sympathetic ganglia of the patient so as to inhibit the cardiorenal disease. In an exemplary embodiment, the method further includes acquiring three dimensional planning image data encompassing the first and second renal arteries, planning an ionizing radiation treatment of first and second target regions using the three dimensional planning image data so as to mitigate the hypertension, the first and second target regions encompassing neural tissue of or proximate to the first and second renal arteries, respectively, and remodeling the target regions by directing the planned radiation from outside the body toward the target regions. | 2012-12-20 |
20120323234 | SURGICAL SYSTEM AND CONTROL PROCESS FOR A SURGICAL INSTRUMENT AND PROCESS FOR CONNECTING BODILY TISSUES - The invention relates to improving a surgical system for connecting bodily tissues, comprising a surgical instrument having two tool elements displaceable relative to each other, each comprising an HF electrode defining a minimum distance from each other, opposite each other, and facing one another in an approach setting of the tool elements, wherein in order for simple and secure connecting of the tissue parts to be connected to each other, the invention proposes that at least one of the HF electrodes is divided into at least two electrode segments and that the at least two electrode segments are electrically insulated from each other. | 2012-12-20 |
20120323235 | METHOD FOR TREATING AN ASTHMA ATTACK - Methods of increasing gas exchange performed by the lung by damaging lung cells, damaging tissue, causing trauma, and/or destroying airway smooth muscle tone with an apparatus inserted into an airway of the lung are disclosed. The damaging of lung cells, damaging tissue, causing trauma, and/or destroying smooth muscle tone with the apparatus may be accomplished via any one of or combinations of the following: heating the airway; cooling the airway; delivering a liquid to the airway; delivering a gas to the airway; puncturing the airway; tearing the airway; cutting the airway; applying ultrasound to the airway; and applying ionizing radiation to the airway. | 2012-12-20 |
20120323236 | METHOD FOR THE CONTROL OF A MEDICAL DEVICE AS A FUNCTION OF NEUTRAL ELECTRODE IMPEDANCE - The method disclosed herein permits the operator of an electrosurgical device to move a safety switch-off threshold for a contact resistance at a neutral electrode from a first value to a second and slightly higher value. This way, for patients with a relatively high resistance yielding a somewhat elevated contact resistance despite correct attachment of the neutral electrode, uninterrupted operation of the device is achievable. | 2012-12-20 |
20120323237 | ASSESSMENT OF ELECTRODE COUPLING FOR TISSUE ABLATION - An electrode catheter and a method for assessing electrode-tissue contact and coupling are disclosed. An exemplary electrode catheter comprises an electrode adapted to apply electrical energy. A measurement circuit is adapted to measure impedance between the electrode and ground as the electrode approaches a target tissue. A processor determines a contact and coupling condition for the target tissue based at least in part on reactance of the impedance measured by the measurement circuit. In another exemplary embodiment, the electrode catheter determines the contact and coupling condition based at least in part on a phase angle of the impedance. | 2012-12-20 |
20120323238 | Tissue Sealing Forceps - A forceps includes an end effector assembly having first and second jaw members. One (or both) of the jaw members is moveable relative to the other between a spaced-apart position and an approximated position for grasping tissue therebetween. One (or both) of the jaw members includes an opposed jaw surface having an electrically-conductive tissue sealing plate disposed thereon. The electrically-conductive tissue sealing plate includes a first portion configured to conduct energy through tissue grasped between the jaw members to create a main tissue seal and a second portion including a plurality of spaced-apart fingers extending from the first portion. The second portion is configured to conduct energy through tissue grasped between the jaw members to create an auxiliary tissue seal extending from the main tissue seal for reducing stress concentrations adjacent the main tissue seal. | 2012-12-20 |
20120323239 | SKULL CLAMP SYSTEM WITH PRESSURE LIMITING AND ALARM SYSTEMS - The skull clamp system with pressure limiting and alarm systems includes at least one and preferably multiple inwardly power driven immobilizing pins adjustably engaging the skull of a patient. The pin power drive systems includes at least one sensor capable of sensing the degree of back pressure on the pin from contact of the pin against the bone of the patient, the sensor being capable of signaling the drive system to stop when the sensor detects a preselected degree of back pressure. The sensor is also capable of signaling an alarm to warn of any reduction of pressure applied to the pins that might result from pin slippage. | 2012-12-20 |
20120323240 | Intramedullary Nail - An intramedullary nail, particular for use with a tibia, may have a proximal end part, a distal end part adapted to be introduced into a medullary space, and a central section. The central section includes a first curved section having a first length with a first radius of curvature, and a second curved section having a second length shorter than the first length and a second radius of curvature smaller than the first radius of curvature. The second radius of curvature may be less than the first radius of curvature. The intramedullary nail also includes a central axis. Tangents at two end points of the central section, including the first and second curved sections, enclose an angle gamma between about 9° and about 12°. The intramedullary nail may have a total length ranging from 200 to 500 mm. | 2012-12-20 |
20120323241 | STERNUM BAND TENSIONER DEVICE, SYSTEM AND METHOD - The invention provides systems and methods for sternum repair. A sternum repair device may include a central body, which may include a plurality of bands and buckles, such that a band extends from the central body and is received by a buckle component. The band may wrap around the sternum and the device may be tightened to keep the separate sternum pieces together. Various band tensioning devices, systems and methods are disclosed. | 2012-12-20 |
20120323242 | SURGICAL AWL AND METHOD OF USING THE SAME - A bone awl is provided for preparing a bone for implantation with a screw. The awl includes a shaft having a first end and a second end opposed to the first end. A handle is fixed to the first end, and an extension extends from the second end. The extension includes a first cutting portion configured to form a hole in bone and a second cutting portion configured to form an internal screw thread in the bone along the surface of the hole. The awl also includes an axial through passage that extends from the handle to the first cutting portion and is dimensioned to receive a Kirshner pin therein. | 2012-12-20 |
20120323243 | DRILL FOR IMPLANT SURGERY - A drill for an implant surgery is provided which allows a mucous membrane in the maxillary sinus to be quickly and safely lifted without being damaged during a surgery for the maxillary sinus. The drill for use in an implant surgery includes a connection portion formed at an upper end of a body of the drill to be connected with a driving device; and a cutting portion formed at a lower end of the body and having a cutting blade for drilling, wherein an outer circumferential edge of a distal end of the cutting portion protrudes rather than a center of the distal end of the cutting portion. | 2012-12-20 |
20120323244 | SYSTEM AND METHOD FOR BONE PREPARATION FOR AN IMPLANT - A computer assisted surgical system for guiding bone cutting operations of an arthroplasty surgery is provided. The computer assisted surgical system includes a cutting guide having a guiding surface for mounting to a bone and a computer. The computer is in communication with the cutting guide and configured to generate a bone model of the first bone without the use of pre-operative bone images, determine a position of an implant model having a bone interface surface on the bone model, determine a position of the cutting guide on the first bone based on the determined position of the implant model on the bone model, and position the guiding surface of the cutting guide to one of a plurality of predetermined cut configurations relative to the bone interface surface. | 2012-12-20 |
20120323245 | CUTTING GUIDE AND METHOD FOR PERFORMING LATERAL RETINACULAR RELEASE - Apparatus and methods are used for severing at least a portion of a lateral retinaculum as part of a lateral release procedure. An elongated guide body has a first, smooth side and second, opposing side having a lengthwise track with a groove. A pushrod having a cutting device is insertable into the track such that the cutting device protrudes from the lengthwise groove, thereby enabling a user to move the pushrod and sever a lateral retinaculum using the cutting device. The cutting device may be a sharp blade or an electrocautery. A method of performing a lateral retinacular release may comprise the steps of inserting the elongated guide body under the skin and subcutaneous fat with the second, opposing side facing a lateral retinaculum; inserting the pushrod into the track of the body; and pushing or pulling the pushrod such that the cutting device severs a lateral retinaculum. | 2012-12-20 |
20120323246 | Patient-Specific Partial Knee Guides And Other Instruments - A patient-specific unicompartmental tibial guide has a patient-specific body with an inner surface. The inner surface is preoperatively configured to nestingly conform and mate in only one position with an anterior portion and a proximal portion of a tibial bone of a specific patient. The tibial guide includes a vertical resection channel having a variable width preoperatively configured for guiding a vertical resection through the proximal portion of the tibial bone. | 2012-12-20 |
20120323247 | SURGICAL ALIGNMENT USING REFERENCES - Methods, systems, and apparatus, including computer-readable storage media, for surgical alignment using references. In one general aspect, a method includes coupling a guide to a joint, the guide defining an axis and having an outer contour formed to substantially conform to a portion of the joint. The first reference is attached at a fixed position relative to the joint. A positioning system is used to determine a position of the axis relative to the first reference, where the position of the axis is determined based upon the position of the guide while the guide is coupled to the joint. The guide is removed from the joint, and after the guide is removed from the joint, an instrument is positioned relative to the axis based on a position of a second reference relative to the first reference. | 2012-12-20 |
20120323248 | ARTHROSCOPIC METHOD AND APPARATUS FOR TISSUE ATTACHMENT TO BONE - Methods are described wherein bone constructs of a patient are used to arthroscopically attach sutures to torn or dysfunctional tissue. A suture or multiple sutures are passed through intersecting/bisecting tunnels formed in the bone. An end of the suture extends from each of the tunnels, and the ends are used to secure the tissue to the bone, such as by arthroscopic tying of the ends, and pulling the tissue against the bone. Devices for performing the methods are also described. | 2012-12-20 |
20120323249 | DRILL GUIDE - A drill guide comprising: a body comprising a hole extending therethrough for guiding a drill; and an alignment tool, the alignment tool being operable to connect the body to an intramedullary rod, such that the orientation of the body is fixable with respect to the intramedullary rod in an anteroposterior plane and in a transverse plane. | 2012-12-20 |
20120323250 | Instrumentation For Recording and Replicating Orthopaedic Implant Orientation - An instrument for recording and replicating the spatial orientation of a dialable component of an implant relative to a bone engaging component of the implant includes a base assembly configured to support the trial implant so that the datum is in a predetermined orientation, a fixture supported on said base assembly, said fixture including an alignment tool configured to engage the first dialable component of the trial implant when the trial implant is supported by said base assembly, and a locking assembly configured to record the angular orientation of said alignment tool relative to said fixture with said alignment tool engaged with the first dialable component, and to replicate the recorded angular orientation with the alignment tool and a second dialable component. | 2012-12-20 |
20120323251 | CROSSING OCCLUSIONS IN BLOOD VESSELS - The present disclosure is directed a method of facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The method may include providing a first intravascular device having a distal portion and at least one aperture and positioning the distal portion of the first intravascular device in the vascular wall. The method may further include providing a reentry device having a body and a distal tip, the distal tip having a natural state and a compressed state and inserting the distal tip, in the compressed state, in the distal portion of the first intravascular device. The method may further include advancing the distal tip, in the natural state, through the at least one aperture of the first intravascular device. | 2012-12-20 |
20120323252 | TIP FOR LEAD EXTRACTION DEVICE - A tip engageable with an elongated sheath member for extracting a cardiac lead from an obstruction in a body vessel of a patient. The tip includes a tip body having a proximal end, a distal end, and a passageway extending therethrough. The tip body proximal end is engageable with the distal end of the sheath member distal end. The passageway of the tip is aligned with the passageway of the sheath such that the cardiac lead is receivable therein. The tip body distal portion has a plurality of sides extending circumferentially therearound, wherein the sides have respective ends and an inwardly directed radiused portion between the ends. | 2012-12-20 |
20120323253 | DEVICE AND METHOD FOR POSITIONING AN ELECTRODE IN TISSUE - A device for positioning an electrode in tissue includes: a lead body having a distal portion; an electrode array coupled to the lead distal portion; an anchoring element having an anchor tip and being operable in a first configuration in which the anchor tip is retracted within the lead and in a second configuration in which the anchor tip is extended outside the lead and configured to fixate within the tissue; and a displacement mechanism that is actuated to bias the electrode array or the anchoring element toward the tissue. A method for positioning an electrode in tissue includes: navigating, to the tissue, a lead with an electrode array, an anchoring element with a distal anchor tip, and a displacement mechanism; biasing the electrode array and anchoring element towards the tissue with the displacement mechanism; and deploying the anchoring element, and verifying fixation of the anchor tip within the tissue. | 2012-12-20 |
20120323254 | MEDICAL ASSEMBLIES AND METHODS FOR IMPLEMENTATION OF MULTIPLE MEDICAL LEADS THROUGH A SINGLE ENTRY - Assemblies and methods provide for implantation of multiple medical leads to a defined space within the body, such as the epidural space, through a single entry. A catheter having multiple lumens or alternatively a single oblong lumen may be used. A distal end of the catheter enters the defined space through the single entry such that the distal ends of the multiple lumens or the oblong lumen are present in the defined space. Medical leads are introduced through the multiple lumens or the oblong lumen into the defined space. In some cases, the distal end of the catheter may be deflectable to direct the medical leads within the defined space. In other cases, sheaths may be present within each lumen of the catheter where the sheaths may be extended into the defined space and deflect to direct the medical leads that are being passed through a lumen of the sheaths. | 2012-12-20 |
20120323255 | LOCALIZATION OF A RADIOACTIVE SOURCE WITHIN A BODY OF A SUBJECT - A system and method is provided for automatic navigation of medical tools. The system can include a tracking system operable to provide information relating to the position of at least a portion of a tool which is inside a body, and an automated navigation system operable to apply forces upon a portion of the tool. The automated navigation system can include a computer operable to store a 3-dimensional route. Furthermore, the automated navigation system can be operable to use the information relating to the position of at least the portion of the tool from the tracking system to apply calculated forces upon the tool, the calculated forces being associated with movement of the tool along the 3-dimensional route. | 2012-12-20 |
20120323256 | ROBOTIC TOOLKIT - A surgical instrument kit comprising: (a) a robotic arm comprising a first jaw including a first bipolar electrode and a second jaw including a second bipolar electrode, wherein at least one of first jaw and second jaw is repositionable with respect to the other jaw; (b) a first surgical tool head including a first electrical load in electrical communication with a first pair of electrical terminals, the first surgical tool head adapted to be removably coupled to the robotic arm; and, (c) a second surgical tool head including a second electrical load in electrical communication with a second pair of electrical terminals, the second surgical tool head adapted to be removably coupled to the robotic arm, where the first pair of electrical terminals of the first surgical tool head are adapted to engage the first bipolar electrode and the second bipolar electrode to establish electrical communication between the first bipolar electrode and a first of the first pair of electrical terminals and between the second bipolar electrode and a second of the first pair of electrical terminals, and where the second pair of electrical terminals of the second surgical tool head are adapted to engage the first bipolar electrode and the second bipolar electrode to establish electrical communication between the first bipolar electrode and a first of the second pair of electrical terminals and between the second bipolar electrode and a second of the second pair of electrical terminals. | 2012-12-20 |
20120323257 | Soft-pedicare - A sponge rubber foot exfoliation apparatus to remove thick, rough, dry, peeling, flaky skin and calluses from the arches, tops, bottoms, sides, heels and toes of feet evenly gently painlessly, smoothly and softly. The first apparatus consisting of a sponge rubber handheld device will attach to a second apparatus. The second apparatus comprising flexible material with abrasives and sponge rubber material affixed with abrasives to exfoliate feet. A single rigid plastic perimeter ring, double rigid plastic plates and single rigid plastic plate of the second apparatus will attach to and secure the flexible and sponge rubber material with abrasives to the first apparatus. | 2012-12-20 |
20120323258 | COMPOSITIONS AND KITS FOR THE REMOVAL OF IRRITATING COMPOUNDS FROM BODILY SURFACES - The invention provides compositions, methods and kits for the removal of harmful or irritating substances from bodily surfaces. Kits may include a composition containing capsaicin and a capsaicin-cleansing composition, e.g., a composition in which capsaicin is soluble. | 2012-12-20 |
20120323259 | KIT AND METHOD FOR EXTRACTING AND STORING A SKIN TISSUE SAMPLE - A kit of components for extracting and storing a skin tissue sample includes an extraction cartridge with a plurality of blades, an actuator cartridge, and a cap with an aqueous preservative. The actuator cartridge is removeably attached to the extraction cartridge and causes the plurality of blades of the extraction cartridge to extract a skin tissue sample from the person. After the skin tissue sample is extracted, the cap is attached to the extraction cartridge to store and suspend the skin tissue sample in an aqueous preservative preloaded in a container in the cap. A liquid-tight seal prevents bodily fluids from contaminating the actuator cartridge and this enables the actuator cartridge to be removed from the extraction cartridge and to be reused. The extraction cartridge and the attached cap, which store the skin tissue sample, are sent to medical laboratory so that the skin tissue sample can be analyzed. | 2012-12-20 |
20120323260 | HAIR REMOVAL APPARATUS - A hair removal apparatus adapted to remove hair from various parts of the body utilizing a threading member. The hair removal apparatus can be manually, electrically, or battery operated, and is configured to fit comfortably within the palm of a user's hand such that the user may accurately guide the hair removal apparatus over the desired hair-removal region. | 2012-12-20 |
20120323261 | SUTURING ASSEMBLY PROVIDING BI-DIRECTIONAL NEEDLE MOVEMENT THROUGH UNI-DIRECTIONAL ACTUATOR MOVEMENT - A suturing assembly includes shaft attached between a handle and a head. The handle includes a brace and an actuator attached to the handle, where the actuator has a neutral position that is distal the brace. The shaft defines a longitudinal axis of the assembly. The head includes a proximal portion housing a needle that is movable through a needle exit port, and a distal end spaced apart from the proximal portion by a throat. The distal end is radially offset from the longitudinal axis and defines a cavity. Movement of the actuator from the neutral position to the brace moves the needle both in a first direction out of the needle exit port into the cavity and in a second direction out of the cavity and into the needle exit port. | 2012-12-20 |
20120323262 | LEFT ATRIAL APPENDAGE TREATMENT SYSTEMS AND METHODS - Embodiments of the present invention encompass systems and methods to prevent complications from atrial fibrillation by preventing or reducing the likelihood of blood flow out of the left atrial appendage, to eliminate a possible source of aberrant electrical circuits, or both. Accordingly, techniques are provided for delivering ligature loops or closure means to the left atrial appendage, and to other anatomical structures of a patient which may be desirable in other surgical procedures. | 2012-12-20 |
20120323263 | SUTURING SYSTEM AND ASSEMBLY - A suturing assembly is provided that is configured to pull a capsule attached to a suture through tissue. The suturing assembly includes a shaft aligned on a longitudinal axis of the suturing assembly, and a head coupled to the shaft. The head includes a proximal portion and a distal end spaced apart from the proximal portion by a throat. The proximal portion houses a needle that is movable through a needle exit port. The proximal portion of the head and the needle exit port are both aligned on the longitudinal axis. A proximal side of the distal end of the head defines a cavity adapted to receive the capsule and a distal side of the distal end of the head defines a slot adapted to allow the suture to pass through the distal end of the head and into the cavity. | 2012-12-20 |
20120323264 | SURGICAL CUTLERY AND MANUFACTURING METHOD THEREOF - A surgical cutlery and a manufacturing method thereof, which prevent over-etching and reduce pierce resistance, are provided. The manufacturing method of the surgical cutlery made of a round bar material | 2012-12-20 |
20120323265 | METHODS FOR DRIVING AN ULTRASONIC SURGICAL INSTRUMENT WITH MODULATOR - Methods for driving a surgical instrument are disclosed. The surgical instrument includes a transducer configured to produce vibrations along a longitudinal axis at a predetermined frequency. An end effector is adapted to couple to the transducer and extends along the longitudinal axis. The end effector includes a body having a proximal end and a distal end. The distal end is movable relative to the longitudinal axis by the vibrations produced by the transducer. A drive module is coupled to the transducer to generate a modulated drive signal. The distal end of the end effector is movable in response to the vibrations produced by the transducer in response to the modulated drive signal. | 2012-12-20 |
20120323266 | Lancet Removal Tool - A lancet removal tool | 2012-12-20 |
20120323267 | OCCLUSION DEVICE AND ASSOCIATED DEPLOYMENT METHOD - An occlusion device for occluding a cavity defined by a body is provided, and includes first and second laterally-expandable portions each formed of a woven tubular fabric and having opposed proximal and distal ends. The first portion is insertable into the cavity so as to be substantially disposed therein upon lateral expansion thereof. A connective element tethers the distal end of the first portion and the second portion, and is cooperable therewith to form a collapsible assembly extending along an insertion axis. Retention members, operably engaged with each of the first and second portions and spaced apart about a laterally outward surface thereof, are adapted to engage the body, after insertion of the collapsed assembly, second portion-first, into the cavity, and subsequent lateral expansion of the first and second portions, so as to retain the assembly substantially within the cavity. An associated deployment method is also provided. | 2012-12-20 |
20120323268 | Three Element Coaxial Vaso-Occlusive Device - A vaso-occlusive device includes inner, intermediate, and outer elements arranged coaxially. The inner element is a filamentous element, preferably a microcoil. The intermediate element is made of a non-metallic material, preferably an expansile polymer. The outer element is substantially non-expansile and defines at least one gap or opening through which the intermediate element is exposed. In a preferred embodiment, when the intermediate element is expanded, it protrudes through the at least one gap or opening in the outer element and assumes a configuration with an undulating, convexly-curved outer surface defining a chain of arcuate segments, each having a diameter significantly greater than the diameter of the outer element. The expanded configuration of the intermediate element minimizes friction when the device is deployed through a microcatheter, thereby reducing the likelihood of buckling while maintaining excellent flexibility. The result is a device with enhanced pushability and trackability when deployed through a microcatheter. | 2012-12-20 |
20120323269 | LUMEN REENTRY DEVICES AND METHODS - A device, such as for use with lumen reentry, including a catheter including a balloon disposed at a distal end thereof, the catheter being formed with a first lumen through the balloon for passing therethrough a guidewire and a second lumen for inflation and deflation of the balloon, the catheter and the balloon being sized and shaped for entry between two layers of a wall of a body lumen, wherein upon expansion of the balloon when placed between the layers, a distal portion of the first lumen that passes through the balloon is bent with respect to a portion of the first lumen proximal to the balloon and is directed towards the body lumen. | 2012-12-20 |
20120323270 | LEFT ATRIAL APPENDAGE OCCLUDER - Systems and methods for occluding a left atrial appendage are disclosed. A left atrial appendage may be covered with a first occluder device to obstruct the passage of blood out of the left atrial appendage. The first occluder device may include an expandable member, a cover attached to and covering an end of the expandable member, and a one-way valve disposed in the cover. The cover may form a flexible pocket between the cover and the expandable member. The cover may be made of bioprosthetic material. A second occluder device may also be disposed within the left atrial appendage by inserting the second occluder device through the one-way valve in the cover of the first occluder device. The second occluder device may be used to stretch the left atrial appendage to obliterate the left atrial appendage. | 2012-12-20 |
20120323271 | FISTULA CLOSURE DEVICES AND METHODS - Described are methods and systems for treating fistulae and other passageways and openings in the body. In certain aspects, an anchored suture is provided that extends from at or near a first fistula opening and through a fistula tract toward a second fistula opening. Various modes of anchoring may be used in this regard including, in some modes, having the suture extend from a deployed anchoring member positioned in and/or around the first opening. The anchored suture, which has a more slender cross sectional dimension relative to the fistula tract through which it extends, is capable of receiving an optional fill substance therealong in the tract. A fill substance can be or include a variety of biodegradable and/or non-biodegradable objects and materials including flowable and non-flowable materials. | 2012-12-20 |
20120323272 | Compound Barb Medical Device and Method - A compound barb medical device is provided which includes an elongated body having at least one barb formed along the length of the body, the barb defining an inner surface with a first portion disposed at a first orientation relative to a longitudinal axis of the elongated body, and a second portion disposed at a second orientation relative to the longitudinal axis. Optionally, the barb defines a third portion disposed at a third orientation relative to the longitudinal axis. A method for forming a compound barb on a medical device is also provided. | 2012-12-20 |
20120323273 | HIGH STRENGTH SUTURE WITH ABSORBABLE CORE AND SUTURE ANCHOR COMBINATION - A novel high tensile strength semi-absorbable composite suture with minimized non-absorbable mass. The suture has a core made from a bioabsorbable polymer. The core is covered by a braided sheath. The braided sheath is made from an absorbable yarn and a bioabsorbable yarn. The bioabsorbable yarn is made from a least one filament of a bioabsorbable polymer. The nonabsorbable yarn is made from at least one filament of ultra high molecular weight polyethylene. | 2012-12-20 |
20120323274 | Biodegradable Shape Memory Polymeric Sutures - Described herein are a group of degradable, thermoplastic polymers, which are able to change their shape after an increase temperature. Their shape memory capability enables bulky implants to be placed in the body through small incisions or to perform complex mechanical deformations automatically. The shape memory polymers are preferably biocompatible and can be biodegradable or non-degradable polymers. Preferably, the biodegradable polymer has a linear degradation rate. In a specifically preferred embodiment, the suture is formed of biodegradable polymer capable of forming a self-tightening knot. In a most preferred embodiment, the suture is used to close a wound or body scission. | 2012-12-20 |
20120323275 | METHOD AND DEVICE FOR APPROXIMATING TISSUE - A wound closure assembly and method for its use. The wound closure assembly includes a curved inserter having a distal end and a proximal end, a filamentary element extending between a proximal end and a distal end, wherein the proximal end is coupled to the proximal end of the curved inserter, a first anchor coupled to the filamentary element between its first and second ends, and a second anchor positioned at the distal end of the filamentary element. The filamentary element is configured to form a slip knot between the first and second anchors so as to enable the distance between the first and second anchors to be decreased by pulling on the proximal end of the filamentary element. The distal end of the curved inserter is received within a channel in the first anchor that extends along its longitudinal length. | 2012-12-20 |
20120323276 | EXPANDABLE INTERSPINOUS DEVICE - Disclosed is a device that is configured to be implanted adjacent interspinous processes of a patient. In one aspect, a spinal implant device comprises: a spacer region adapted to be positioned between first and second spinous processes of first and second vertebral bodies to limit movement of the first spinous process and the second spinous process toward one another; and an attachment region attached to the spacer region, the attachment region adapted to attach to the first spinous process via a fastener, the attachment region comprising a pair of pads having attachment elements that are configured to attach onto the spinous process | 2012-12-20 |
20120323277 | Spinal Facet Implants with Mating Articulating Bearing Surface and Methods of Use - Superior and/or inferior facets of one or more facet joints may be replaced by superior and/or inferior facet joint prostheses. In one embodiment, a kit of superior or inferior prostheses is provided, in which the prostheses have at least two dimensions that vary among members of the kit independently of each other. Each prosthesis may have a bone engaging surface having a surface that is polyaxially rotatable against a corresponding resection of a vertebra. Each prosthesis may also have an articulating surface shaped such that, after attachment to the spine, the replaced or partially replaced facet joints provide a larger medial-lateral range of motion when the spine is flexed than when the spine is extended. Crosslinks may be used to connect left and right prosthesis together in such a manner that they are stabilized in a position in which they are seated directly against the vertebra. | 2012-12-20 |
20120323278 | MINIMALLY INVASIVE SPINAL STABILIZATION SYSTEM - A spinal fixation assembly includes a pedicle rod and pedicle screws which secure the pedicle rod to the spine. Each pedicle screw includes a head configured to receive a portion of the pedicle rod, and a threaded portion extending from a first end of the head and configured to engage a vertebra. The pedicle rod is secured to the head by a fastener. The head includes a breakaway region that defines a location in which at least a first portion of the head can be easily separated from the remainder of the head upon application of sufficient force to the first portion. A minimally invasive method of implanting the spinal fixation assembly is disclosed. | 2012-12-20 |
20120323279 | MINIMALLY INVASIVE SPINAL STABILIZATION METHOD - A spinal fixation assembly includes a pedicle rod and pedicle screws which secure the pedicle rod to the spine. Each pedicle screw includes a head configured to receive a portion of the pedicle rod, and a threaded portion extending from a first end of the head and configured to engage a vertebra. The pedicle rod is secured to the head by a fastener. The head includes a breakaway region that defines a location in which at least a first portion of the head can be easily separated from the remainder of the head upon application of sufficient force to the first portion. A minimally invasive method of implanting the spinal fixation assembly is disclosed. | 2012-12-20 |
20120323280 | METHODS, TOOLS AND DEVICES FOR SPINAL FIXATION - A method for spinal rod insertion includes providing a U-shaped hook tool comprising first and second legs, and inserting the first leg into a first location of a first vertebra and then pushing the hook tool along an arc-shaped path until the first leg exits through a second location of an adjacent second vertebra. Next, providing a spinal stabilization rod and a folded flexible wire comprising first and second open ends at the front end and a closed loop end. The closed loop end is attached to a first end of the spinal stabilization rod and the first and second open ends of the folded flexible wire are inserted into an open end of the second leg of the hook, and the folded flexible wire is threaded through the U-shaped hook and the first and second open ends of the flexible wire exit through an open end of the first leg. | 2012-12-20 |
20120323281 | Method of Implanting a Modular Fracture Fixation System - A fracture fixation plate system for use on a long bone having a metaphysis and a diaphysis, includes at least one end plate having a head portion for the metaphysis, and at least one diaphyseal plate having a first end and a second end with a plurality of screw holes therebetween. The end plate includes mating structure adapted to mate with and securely couple to at least one end of the at least one diaphyseal plate. The system preferably includes several end plates and diaphyseal plates to accommodate anatomy of various sizes. A method for coupling the plates to the bone is also provided. | 2012-12-20 |
20120323282 | METHOD FOR DESIGNING AND/OR OPTIMIZING A SURGICAL DEVICE - A method for designing and/or optimizing an implant that has one or more through holes with a central axis for receiving a bone fixation element. The method includes: providing a general collection of three-dimensional bone quality data obtained from a patient population; identifying in the patient population N>2 categories of patients with significantly different N>2 homologous sub-collections of bone quality data; and designing an implant or optimizing an existing implant for each of the N>2 sub-collections such that the at least one through hole is located at an optimal place and with an optimal direction of the central axis relative to the implant. The optimal position and direction is chosen based on each of the N>2 sub-collections of data so as to obtain an optimal anchorage of the bone fixation element in the bone when introduced through the through hole. | 2012-12-20 |
20120323283 | BONE FIXTURE ASSEMBLY - An assembly for rigid bone fixation includes a plate and a screw. The screw can be rotated freely within the plate in a non-locking configuration to secure the plate against the bone. A locking mechanism is engaged to prevent the screw from moving relative the plate. In one embodiment, the plate includes a threaded portion and a non-threaded portion. The screw head rotates within the non-threaded portion to tighten the screw and pull the plate against the bone. The locking mechanism can include a moveable nut that rotates within the threaded portion of the plate to lock the screw and plate in a locking mode. The assembly can be used for rigid fixation of bones that experience cyclic loads, such as the sternum and mandible. Methods of rigid bone fixation are also described. | 2012-12-20 |
20120323284 | VARIABLE ANGLE LOCKING IMPLANT - A variable angle locking implant includes a bone plate having a lower surface, an upper surface, and at least one opening extending from the lower surface to the upper surface along an axis. The opening has a plurality of fins oriented along a plane. The axis is non-perpendicular to a tangent of a projection of the lower surface across the opening, the tangent defined at the intersection between the axis and the projected lower surface, and/or the plane is non-parallel to the tangent. The implant includes at least one fastener, and the plurality of fins are deflectable relative to a head portion of the fastener such that the fastener can be inserted and retained at any one of a plurality of angles. | 2012-12-20 |
20120323285 | BONE SCREW - A bone screw including a main body portion having a proximal end and a distal end. An external threaded surface and an internal threaded surface are formed on the main body portion. The external threaded surface intersects the internal threaded surface proximate a lower surface of the external threaded surface and a lower surface of the internal threaded surface. A plurality of bone growth apertures is defined on the surface of the main body portion where the external threaded surface and the internal threaded surface are not located. The bone growth apertures comprise between about 10 percent and about 60 percent of the surface of the main body portion. | 2012-12-20 |
20120323286 | DEVICE FOR THE DISTRACTION OF A BONE SEGMENT - A device for distraction of a bone segment from local bone, or endo-distractor. The device has a rotatable, smooth shaft adjoined by a straight anchoring screw. During the unscrewing of the anchoring screw a carrier piece transfers the axial movement but not the rotation to the bone segment. The carrier piece for the bone segment is a pressure plate which is formed with an open slit and which, by being pushed orthogonally, with respect to the longitudinal direction of the shaft, onto the shaft, can be secured on the latter in the axial direction. | 2012-12-20 |
20120323287 | IMPLANT TO STRESS BONE TO ALTER MORPHOLOGY - An implant operable to alter morphology of a long bone can comprise a first longitudinal member, a second longitudinal member, and an adjusting member. The first longitudinal member can have a bone attachment end and a first connecting end. The second longitudinal member can have a second bone attachment end and a second connecting end. The adjusting member can connect to both of the first and second connecting ends. The adjusting member can be selectively moveable from a first implanted position where the first and second connecting ends are fixed to respective ends of the long bone and spaced apart a first distance to a second implanted position where the first and second connecting ends are fixed to the respective ends of the long bone and spaced apart a second distance. The second distance is less than the first distance causing a long bone to be compressed between the first and second bone attachment ends. | 2012-12-20 |
20120323288 | HYBRID CLUSTERED NEURAL INTERFACE SYSTEM - An apparatus comprises a flexible substrate. The flexible substrate includes a first substrate surface, a surface electrode array that includes a plurality of electrodes disposed on the first substrate surface, one or more flexible neural probes substantially orthogonal to the first substrate surface and insertable into biological tissue, and a penetrating electrode array that includes a plurality of electrodes formed on the one or more flexible neural probes, wherein electrodes of the surface electrode array and the penetrating electrode array are configured to one or both of receive a neural signal from a neural signal source and provide electrical stimulation energy to a neural stimulation target. | 2012-12-20 |
20120323289 | METHOD AND APPARATUS FOR ESTABLISHING CONTEXT AMONG EVENTS AND OPTIMIZING IMPLANTED MEDICAL DEVICE PERFORMANCE - An apparatus and method for adjusting the performance of an implanted device based on data including contextual information. Contextual information, including operational and performance data concerning the implanted device as well as the patient with the implanted device, is stored by a portable electronic device. In one embodiment, the portable electronic device is adapted for battery operation and includes a personal digital assistant (PDA). The portable electronic device is adapted for use as an interface to conduct wireless communications with the implanted device. In one embodiment, the portable electronic device interfaces with a clinical programmer for use by a physician. | 2012-12-20 |
20120323290 | Methods and Devices for Adapting Charge Initiation for an Implantable Defibrillator - Adaptive methods for initiating charging of the high power capacitors of an implantable medical device for therapy delivery after the patient experiences a non-sustained arrhythmia, and devices that perform such methods. The adaptive methods and devices adjust persistence criteria used to analyze an arrhythmia prior to initiating a charging sequence to deliver therapy. Some embodiments apply a specific sequence of X-out-of-Y criteria, persistence criteria, and last event criteria before starting charging for therapy delivery. | 2012-12-20 |
20120323291 | Method and Apparatus to Perform Electrode Combination Selection - Approaches for selecting an electrode combination of multi-electrode pacing devices are described. Electrode combination parameters that support cardiac function consistent with a prescribed therapy are evaluated for each of a plurality of electrode combinations. Electrode combination parameters that do not support cardiac function are evaluated for each of the plurality of electrode combinations. An order is determined for the electrode combinations based on the parameter evaluations. An electrode combination is selected based on the order, and therapy is delivered using the selected electrode combination. | 2012-12-20 |
20120323292 | SYSTEM FOR NEURAL CONTROL OF RESPIRATION - A system, device and method for neural control of respiration are provided. One aspect of this disclosure relates to an implantable medical device for sensing and controlling respiration during incidence of central respiratory diseases. According to various embodiments, the device includes a sensing circuit to receive sensed signals representative of an incidence of a central respiratory disease. The device also includes a neural stimulator adapted to generate neural stimulation signals, and a controller to communicate with the sensing circuit and to control the neural stimulator to stimulate a desired neural target in response to the detection of the incidence of a central respiratory disease. In an embodiment, the device includes a plurality of sensors which are adapted to monitor physiological parameters to detect the incidence of a central respiratory disease and to send signals to the sensing circuit. Other aspects and embodiments are provided herein. | 2012-12-20 |
20120323293 | DEVICE AND METHOD FOR TREATING DISORDERS OF THE CARDIOVASCULAR SYSTEM OR HEART - A device and method are provided to treat heart failure by stimulating to cause diaphragm contraction. | 2012-12-20 |
20120323294 | PERCUTANEOUS TIBIAL NERVE STIMULATOR - A tibial nerve stimulation device including a percutaneous electrode for inserting adjacent a stimulation site of a patient and a neurostimulator unit attachable to a transcutaneous electrode configured to be applied to skin adjacent the stimulation site. The neurostimulator unit includes a pulse generator electrically coupled to the percutaneous needle electrode and transcutaneous electrode and a microcontroller in communication with the pulse generator for monitoring a number of available treatment credits and activating the pulse generator, each available treatment credit corresponding to a treatment session and the pulse generator operable to be activated for performing the treatment session when the number of available treatment credits is at least one. A computer system is operable to communicate with the microcontroller of the neurostimulator unit for receiving a treatment credit request and transmitting the number of treatment credits purchased to the microcontroller of the neurostimulator unit. | 2012-12-20 |
20120323295 | SCANNING MECHANISM AND TREATMENT METHOD FOR LLLT OR OTHER LIGHT SOURCE THERAPY - A scanning mechanism to scan a light source, such as a low-level laser, to create a desirable energy distribution on a treatment area. The light source may include multiple light beam generators, each having a different wavelength and each having a different energy distribution. The scanning mechanism can be programmable to scan in different patterns in accordance with a desired treatment. | 2012-12-20 |
20120323296 | BRAIN COOLING APPARATUS AND BRAIN COOLING DEVICE SUITABLE THERETO - A brain cooling apparatus is provided that can circulate a fluid between a containing unit of a brain cooling device and the brain cooling apparatus while maintaining an appropriate pressure of the fluid in the containing unit, and a brain cooling device suitable thereto also is provided. A control device circulates a physiological saline solution between a storage tank and a cuff by driving a first pump in a direction in which the physiological saline solution flows toward the cuff, and driving a second pump in a direction in which the physiological saline solution flows toward the storage tank. In this state, the control device adjusts the rotation speed of at least the second pump, so that the pressure of the physiological saline solution in the cuff becomes a preset target pressure. | 2012-12-20 |
20120323297 | LEADS WITH HIGH RESISTIVE SURFACE - Implantable medical leads having resistance characteristics adapted to dissipate radio frequency (RF) electromagnetic energy during medical procedures such as magnetic resonance imaging (MRI) are disclosed. An illustrative medical device includes a lead having an inner electrical conductor operatively coupled to an electrode and a pulse generator, and one or more outer resistive shields that radially surround the inner conductor and dissipate RF energy into the surrounding body tissue along the length of the lead. | 2012-12-20 |
20120323298 | SHAPE MEMORY ALLOY ARTICLES WITH IMPROVED FATIGUE PERFORMANCE AND METHODS THEREFORE - Articles made of shape memory alloys having improved fatigue performance and to methods of treating articles formed from shape memory alloy materials by pre-straining the articles (or desired portions of the articles) in a controlled manner so that the resultant articles exhibit improved fatigue performance. The shape memory articles are preferably medical devices, more preferably implantable medical devices. They are most preferably devices of nitinol shape memory alloy, most particularly that is superelastic at normal body temperature. The pre-straining method of the present invention as performed on such articles includes the controlled introduction of non-recoverable tensile strains greater than about 0.20% at the surface of a desired portion of a shape memory alloy article. Controlled pre-straining operations are performed on the shape-set nitinol metal to achieve non-recoverable tensile strain greater than about 0.20% at or near the surface of selected regions in the nitinol metal article. | 2012-12-20 |
20120323299 | ROTATIONAL ALIGNMENT WIRE SYSTEM FOR AN ENDOVASCULAR DELIVERY SYSTEM - An endovascular delivery system includes an endovascular prosthetic device and a signal active guide wire engaging the endovascular prosthetic device. A rotary encoder is coupled with the guide wire and the endovascular prosthetic device to provide an encoder signal on the guide wire. The encoder signal is indicative of axial angular position of the endovascular prosthetic device during implantation of the endovascular prosthetic device in a body of a patient. | 2012-12-20 |