52nd week of 2009 patent applcation highlights part 53 |
Patent application number | Title | Published |
20090318951 | EMBOLUS BLOOD CLOT FILTER DELIVERY SYSTEM - A blood filter delivery system for delivering a blood filter into a vein includes a push rod for pushing the blood filter through and out of a catheter, the push rod having a filter positioning assembly on one end. The filter positioning assembly includes positioner members, which retain anchor members of the filter. The filter positioning assembly can position the end of the delivery catheter near the blood vessel centerline before releasing the filter's anchor members, thereby helping to align the blood filter along the centerline of the blood vessel. | 2009-12-24 |
20090318952 | DEVICE AND METHOD FOR COMPRESSING WOUNDS - A dressing for applying compression to a wound in a patient includes a bladder having a non-deformable end wall and a deformable membrane. The dressing may include a flexible web having an adhesive layer on one side thereof for securing the dressing to the patient so as to hold the bladder against the patient's skin. Upon inflation, the deformable membrane projects towards the patient's skin and exerts pressure on the wound to reduce the flow of blood from the wound. | 2009-12-24 |
20090318953 | DEVICE AND METHOD FOR COMPRESSING WOUNDS - A dressing for applying compression to a wound in a patient includes a bladder having a non-deformable end wall and a deformable membrane. The dressing may include a flexible web having an adhesive layer on one side thereof for securing the dressing to the patient so as to hold the bladder against the patient's skin. Upon inflation, the deformable membrane projects towards the patient's skin and exerts pressure on the wound to reduce the flow of blood from the wound. | 2009-12-24 |
20090318954 | SYSTEM AND METHOD FOR ACTUATING A LAPAROSCOPIC SURGICAL INSTRUMENT - The invention is directed to a pin and slot design where the driving slots are moved from the tips to the actuation rod in one aspect of the invention. As a result, the back end of each blade or tip can be dramatically reduced in area so that during full deflection, very little or no part of the blade or tip extends beyond the outside diameter of the shaft. This ensures that nothing catches on the blades or tips during grasper use and the shrink tubing found on the scissors would not be deformed. This can be done because the area for the slots is not needed. Moreover, the usable area for the drive slots on the blade or tip of the actuation rod is maximized to the overall diameter of the outer tube or shaft which provides additional leverage to the blades or tips. In addition, the depth of each slot can be varied such that during actuation, increased tension can be put on the blades or tips throughout the cut. More specifically, the surgical instrument of the invention comprises an elongate tube extending along an axis including an actuation rod coaxially slidable within the elongate tube, a first tip including a first pin formed on a proximal end surface of the first tip, and a second tip including a second pin formed on a proximal end surface of the second tip, the second tip pivotally connected to the first tip at a common pivot pin operably connected to the elongate tube to open and close the tips in response to movement of the actuation rod. The actuation rod has a slot to accept the pins of the first and second tips, the slot has camming surfaces for the pins to slide within the slot, and the proximal ends of the tips extend minimally outside the diameter of the elongate tube during actuation of the tips. | 2009-12-24 |
20090318955 | VASCULAR CLOSURE DEVICE - The present invention provides a porous structure that works very effectively to seal a puncture site with optimum porosity, absorbent capacity and perfect anatomical fit. The plug density and other fiber properties/geometry (total denier; number of filaments; etc) have provided an efficient structure that allows instantaneous absorption of blood during deployment. The final size of the plug with absorbed fluids provides an anatomical fit and seals the puncture site within few minutes after deployment. | 2009-12-24 |
20090318956 | Wire-Like And Other Devices For Treating Septal Defects And Systems And Methods For Delivering The Same - Systems, devices and methods for treating internal tissue defects, such as septal defects, with implantable devices are provided. In some exemplary embodiments, these devices include one or more wires coupled together. The device can include deflectable anchors for engaging the septal tissue. | 2009-12-24 |
20090318957 | EXPANDABLE BACKSPAN STAPLE - A staple having an expandable backspan and a pair of spaced legs is described. The expandable backspan is configured to expand or deform to accommodate tissues of varying thicknesses. In one embodiment, the backspan is non-linear and defines a recess. In another embodiment, the backspan includes a deformable pad or spacer. The amount of deformation of the backspan is proportional to the thickness of the tissue, i.e., the greater the thickness of tissue, the greater the deformation of the backspan. | 2009-12-24 |
20090318958 | METHOD OF SUTURING - The invention relates to a method of suturing. Briefly, a portion of a needle having a continuous suture thread running through the eye is advanced through a first location on a first side of a tissue. When the needle is withdrawn from said tissue a suture loop is retained on a second side of said tissue. This can be repeated to obtain as many suture loops as desired on additional locations of the tissue. When all the desired suture loops are formed the needle is advanced all the way through the tissue and a single strand of suture thread is passed through each suture loop on the second side of the said tissue. Thus, one continuous suture forms the suture loop(s) and engages the sutured loops. In a preferred embodiment the needle eye, through which the suture thread runs, is located in the tip portion of said needle. It is also preferred that the needle is curved. The tissue may be, for example, a tendon (e.g., patellar), a ligament, or a graft. In yet another embodiment the suturing method of the present invention involves passing a suture through a tendon to achieve maximum suture fixation strength, as well as a method of securing the tendon to bone that allows for accelerated tendon healing to bone. The invention also relates to a construct prepared by the suture methods of the present invention. | 2009-12-24 |
20090318959 | TECHNIQUE FOR TISSUE FIXATION BY CAPTURING AND ANCHORING A LINK OF SUTURE CHAIN ATTACHED TO TISSUE - A method and device for knotless fixation of tissue. The method utilizes a push-in type anchor (for example, a self-punching anchor) and a suture chain that includes a plurality of loops. A first portion of the suture chain is secured to the tissue to be fixated. The suture chain is next secured to the push-in type anchor (for example, by passing the suture chain through an eyelet of the anchor). The anchor is then advanced along the suture chain to bring a tip of the anchor above a chosen loop or link of the suture chain. The tip of the anchor is pushed through the chosen loop so that the tip locks the chosen loop in place (for example, by capturing both sides of the link above a shoulder of the anchor). With the captured link, the anchor is advanced into a pilot hole or socket formed in the bone to fixate the tissue. The captured link provides a hard stop that does not slip, in addition to frictional interference between the anchor and the bone socket. | 2009-12-24 |
20090318960 | METHOD OF KNOTLESS TISSUE FIXATION WITH CRISS-CROSS SUTURE PATTERN - A knotless tissue fixation (such as an arthroscopic rotator cuff repair) with a criss-cross suture pattern. The criss-cross pattern is obtained by (i) providing a first medial row constructed with a first plurality of fixation devices, at least one of the first plurality of fixation devices being an anchor; (ii) providing a second lateral row constructed with a second plurality of fixation devices, at least one of the second plurality of fixation devices being a knotless fixation device; and (iii) providing a structure formed of suture, suture chain, tape or allograft/biological component, and extending the structure in a criss-cross pattern, over the soft tissue, so that the structure is secured in place by the anchors. | 2009-12-24 |
20090318961 | Method and Apparatus for Coupling Soft Tissue to a Bone - A method and apparatus for surgically repairing a tear in soft tissue is disclosed. A plurality of collapsible tubes are positioned about the suture. The collapsible tubes are pushed through soft tissue and orthopedic mesh on opposite sides of a tear in soft tissue. When tension is applied to the suture, the tubes are compressed to fix the suture to the soft tissue and draw the soft tissue portions together. | 2009-12-24 |
20090318962 | SURGICAL SUTURES INCORPORATED WITH STEM CELLS OR OTHER BIOACTIVE MATERIALS - Materials and Methods for immobilizing bioactive molecules, stem and other precursor cells, and other agents of therapeutic value in surgical sutures and other tissue scaffold devices are described herein. Broadly drawn to the integration and incorporation of bioactive materials into suture constructs, tissue scaffolds and medical devices, the present invention has particular utility in the development of novel systems that enable medical personnel performing surgical and other medical procedures to utilize and subsequently reintroduce bioactive materials extracted from a patient (or their allogenic equivalents) to a wound or target surgical site. | 2009-12-24 |
20090318963 | SPINNING SOLUTION COMPOSITION, PROCESS FOR PRODUCING REGENERATED SILK FIBER USING THE COMPOSITION, AND REGENERATED SILK FIBER PRODUCED BY THE PROCESS - A spinning solution composition which provides regenerated silk fiber that exhibits a strength and elongation close to those of natural silk fiber, is rapidly degradable in vivo, and can be caused to have ability to gradually release a drug to prevent inflammation; a process for producing such regenerated silk fiber by use of the composition; and regenerated silk fiber obtained through the process. | 2009-12-24 |
20090318964 | KNOTLESS SUTURE ANCHOR - An anchoring device for deployment in a pre-formed hole to secure soft tissue to bone. Embodiments of the anchoring device include an outer member and an inner member that moves relative to the outer member from a suture-unlocked position to a suture-locked position. The inner member further includes an elongated projection with a proximal end that defines an outer dimension. In one embodiment, the elongated projection is configured to interface with a portion of the outer member so as to change the outer dimension in a manner that causes the elongated projection to displace a portion of the bone. | 2009-12-24 |
20090318965 | TECHNIQUE FOR TISSUE FIXATION BY REELING IN AND ANCHORING SUTURE ATTACHED TO TISSUE - A method and device for knotless fixation of tissue. The method utilizes a push-in type anchor (for example, a self-punching anchor) and a suture chain that includes a loop or a plurality of loops. A first portion of the suture chain is secured to the tissue to be fixated. The suture chain is next secured to the push-in type anchor (for example, by passing the suture chain through an eyelet of the anchor). The anchor is then advanced along the suture chain to bring a tip of the anchor above a chosen loop or link of the suture chain. The tip of the anchor is pushed through the chosen loop so that the tip locks the chosen loop in place (for example, by capturing both sides of the link above a shoulder of the anchor). With the captured link, the anchor is advanced into a pilot hole or socket formed in the bone, and then the anchor is rotated within the hole or socket to reel in the suture chain and to tension, therefore, the suture chain. | 2009-12-24 |
20090318966 | SYSTEM AND METHOD FOR ATTACHING SOFT TISSUE TO BONE - Disclosed herein are methods and devices for securing soft tissue to a rigid material such as bone. A bone anchor is described that comprises a base and a top such that suture material may be compressed between surfaces on the base and top to secure the suture to the anchor. Also described is an inserter that can be used to insert the bone anchor into bone and move the anchor top relative to the anchor base to clamp suture material there between. Also described is a soft-tissue and bone piercing anchor and associated inserter. Methods are described that allow use of the bone anchors to provide multiple lengths of suture material to compress a large area of soft tissue against bone. | 2009-12-24 |
20090318967 | Spacer for use in a surgical operation for spinous process of spine - A spacer used for maintaining an interval between spinous processes of spine, capable of preventing unnecessary damage to vertebras, simplifying the surgical operation, and reducing the time taken for the surgical operation by implementing a new vertebra fastening means for strongly maintaining a state of extending an interval between spinous processes by using a shape memory material which can be restored by body temperature. In addition, such a spacer may be capable of easily insertion in a lateral direction, thereby reducing a cut portion for the surgical operation and avoiding unnecessary cutting of a ligament fastening the spinous processes. In addition, there is provided a spacer for use in a surgical operation for spinous processes of spine, capable of enabling the spine to move according to patient's movement by providing an elastic vertebra fastening means, so that the patient can move smoothly after the surgical operation. | 2009-12-24 |
20090318968 | SYSTEMS AND METHODS FOR POSTERIOR DYNAMIC STABILIZATION - A system for providing dynamic stabilization and balance control at a vertebral motion segment has first and second bridge elements and at least one bias element. The bridge elements anchor to adjacent vertebrae with polyaxially adjustable anchoring members, and the bias elements attach to each bridge element to span between them. Each bias element has two fixation portions and a bias body extending between the fixation portions. Each bias element may comprise an elastically deformable material to provide dynamic stabilization with motion, or may comprise rigid material to provide rigid stabilization, and both bias element types may be included in one system. The bias elements are attachable to the bridge elements at discrete attachment locations, or at non-discrete attachment locations. Alternate embodiments may include three or more bridge elements on adjacent vertebrae, and multiple bias elements. A tensioning tool may provide adjustable tension to an elastically deformable bias element. | 2009-12-24 |
20090318969 | BONE ANCHORING ASSEMBLY - A bone anchoring assembly includes a bone anchoring element having a shank to be anchored in a bone or a vertebra, and a receiving part for receiving a rod. The assembly includes a rod made at least partly of a material which exhibits a material flow under pressure. The receiving part includes a channel with an approximately U-shaped cross-section with two free legs, a first locking element cooperating with the legs to secure the rod in the channel, and a second locking element cooperating with the first locking element and acting independently from the first locking element onto the rod. A pin-shaped projection is provided at the second locking element which comes into contact with the rod when tightening the second locking element, and at least one pin-shaped projection is provided in the channel which comes into contact with the rod when tightening the first locking element. | 2009-12-24 |
20090318970 | Spinal Rod Connectors Configured to Retain Spinal Rods of Varying Diameters - A spinal rod connector is configured to accommodate a range of spinal rod diameters. The present spinal rod connector may take the form of a spinal rod screw head, hook, spinal rod connector or a spinal rod holder. The spinal rod connector has spinal rod reception slots whose sides narrow towards a bottom of the slot. The narrowing of the sides provides a wedging effect such that a spinal rod is wedged into place during locking. The narrowing sides of the slots thus provide for the accommodation of varying rod diameters. The spinal connector also provides significant improvement in spinal rod torsional resistance compared to prior art radial shaped slots. In one form, the spinal rod reception slots are essentially V-shaped. However, other shapes following the principles of the present invention may be used and are contemplated. The width of the slot sides and the rate of curvature of the slot sides thus determine the range of spinal rod diameters that are accommodated by the spinal rod reception slots and therefore the spinal rod connector. | 2009-12-24 |
20090318971 | INTERVERTEBRAL STABILIZATION SYSTEM - An intervertebral stabilization system for at least three vertebrae comprising
| 2009-12-24 |
20090318972 | Spinal fixation tool set and method - A spinal implant tool set includes end guide tools having flexible back wall flaps that receive opposite ends of the rod and intermediate guide tools that hold the rod in intermediate locations between the end guide tools. Both the end and intermediate guide tools include an attachment structure for operably connecting the guide tool to a bone screw. A multi-function installation tool and a bone screw driver each mate and cooperate with the guide tools. A method utilizing the tool set allows a surgeon to percutaneously implant the bone screws and the rod in the patient. | 2009-12-24 |
20090318973 | BONE FIXING DEVICE - The invention concerns a bone fixing device ( | 2009-12-24 |
20090318974 | Device For Securing Spinal Rods - A device is disclosed for securing a spinal rod to the spine which includes a head portion configured to receive a spinal rod, a locking cap configured to engage the head portion and the spinal rod upon rotation of the locking cap relative to the head portion to secure the position of the head portion relative to the spinal rod, and a fastener portion depending from the head portion and configured to engage the spine. Methods of utilizing such a device are also disclosed. | 2009-12-24 |
20090318975 | Rod Reducer Method - A method of operating a rod reducer includes connecting a cam coupling rod reducer to a screw head of a pedicle screw assembly, wherein spaces in between prongs at a second end of an inner tube of the rod reducer are positioned parallel to a rod of the pedicle screw assembly, and wherein the connection of the cam coupling rod reducer to the screw head indicates a first position of operation; rotating a lever cam of the cam coupling rod reducer until an indication line marked on an outer body of the cam coupling rod reducer moves to a second position of operation; and rotating the lever cam to a third position of operation, wherein the third position of operation indicates that the rod is optimally seated in the pedicle screw assembly, and that the pedicle screw assembly is ready to accept a blocker screw. | 2009-12-24 |
20090318976 | IMPLANTABLE BRACE FOR PROVIDING JOINT SUPPORT - Internal braces and methods of implanting same. A brace can be implanted on one side of a joint, or a pair of braces can be implanted, one on each opposite side of a joint. Each brace supports the joint over at least a portion of its range of motion. Distraction may be provided, or load sharing can be accomplished without distraction. Relative axial rotation of the bones connected by the brace may be permitted. One or more compliant members may be provided in the brace. | 2009-12-24 |
20090318977 | WEDGED PROFILE PLATE - A bone plate used in conjunction with various procedures to correct certain deformities, such as a Latarjet procedure. The bone plate is provided with a plurality of spikes having a truncated, pyramidal shape with a plurality of sides or faces that converge to a tip line. The height of each spike is of about 2.5 to about 3 mm. The design of the spikes allows the plate to stay in the right position by simply pressing the plate with the fingers on the bone or using a specific instrument (before the fixation holes are drilled and the fixation devices such as screws are secured). The bone plate may be provided with side, lateral faces that have a non-uniform width (i.e., a wedged profile) to allow for orthograde placement of the fixation device, even in the case of angled bone surfaces. | 2009-12-24 |
20090318978 | IMPLANTABLE ORTHOPAEDIC DEVICE, IN PARTICULAR FOR THE CERVICAL SPINE - The invention relates to an implantable orthopaedic device, in particular for the cervical spine, of the type formed by a support plate ( | 2009-12-24 |
20090318979 | Locking Plate Benders - A system for contouring a locking plate includes a locking plate and at least one bender. The locking plate includes a plurality of threaded screw holes connected to one another by one or more ribs. The at least one bender includes a threaded tip configured to threadably engage one or more of the plurality of threaded screw holes and a shoulder operable to transmit mechanical force to the locking plate once the threaded tip is threadably engaged with one of the plurality of threaded screw holes. | 2009-12-24 |
20090318980 | PERCUTANEOUS FACET FIXATION SYSTEM - A percutaneous facet fixation system minimally invasive, reproducible, efficient, and effective. Capable of immediate stabilization of a facet joint complex, the instrumentation and methods may be used with C-arm and/or endoscopic visualization. | 2009-12-24 |
20090318981 | PIN ASSEMBLY FOR OPERATION - A pin assembly for operation includes a hollow pin for operation having a plurality of side holes defined through a wall thereof and a root part which is closed or open due to the presence of a through-hole; and a hollow support member having a pin fastening part formed therein in the shape of a groove to fasten one end of the pin for operation, and being open at both ends thereof, wherein the pin for operation is fastened to the pin fastening part of the support member, and by applying external force to one end of the support member, the pin for operation is inserted into a bone. | 2009-12-24 |
20090318982 | METHODS OF INJECTING CALCIUM BASED NEUTRAL AND BIORESORBABLE BONE GRAFTS - An injectable and moldable putty comprising biodegradable calcium-based compounds including calcium sulfate, hydroxyapatite, and tricalcium phosphate is invented. The putty hardens into a solid body when mixed with water, saline, serum, or other neutral aqueous solutions. The hardening time of the putty can be tailored in order to meet the specific requirements of various dental or orthopedic applications. The pH of the putty is neutral during and after mixing. The invented putty may be used as bone graft, bone implant, or implantable drug delivery device. | 2009-12-24 |
20090318983 | METHOD AND APPARATUS FOR DETECTION AND TREATMENT OF AUTONOMIC SYSTEM IMBALANCE - Method and apparatus for preventing autonomic system disturbances by recording physiological parameters, measuring beat-to-beat variability of these parameters, and using the measured beat-to-beat variability to control the delivery of drug therapy and electrical impulses to the heart. | 2009-12-24 |
20090318984 | EXTERNAL PACEMAKER WITH AUTOMATIC CARDIOPROTECTIVE PACING PROTOCOL - A pacing system includes a pacemaker and a pacing protocol module externally attached to the pacemaker. The pacing protocol module stores the pacing protocol. The pacemaker controls delivery of pacing pulses by automatically executing the pacing protocol. In one embodiment, the pacing protocol is a cardioprotective pacing protocol for preventing and/or reducing cardiac injury associated with myocardial infarction (MI) and revascularization procedure. The pacing pulses are generated from the pacemaker and delivered through one or more pacing electrodes incorporated onto one or more percutaneous transluminal vascular intervention (PTVI) devices during the revascularization procedure. | 2009-12-24 |
20090318985 | METHOD AND APPARATUS FOR CONTROLLING ANTI-TACHYARRHYTHMIA THERAPY USING HEMODYNAMIC TOLERABILITY - A cardiac rhythm management system identifies a relationship between one or more hemodynamic parameters sensed from a patient and levels of hemodynamic tolerability of the patient. The identified relationship allows an implantable medical device to control delivery of anti-tachyarrhythmia therapy using the patient's hemodynamic tolerability during a detected tachyarrhythmia episode, in addition to classifying the detected tachyarrhythmia episode by its type and origin. | 2009-12-24 |
20090318986 | Systems, Methods and Apparatus for Treating Cardiac Dysfunction with Neurostimulation - Methods, systems, and apparatus for the treatment of heart failure (both systolic and diastolic), hypertension, and arrhythmia in patients by stimulating one or more nerves, particularly peripheral nerves, using neurostimulation are described. The therapeutic treatment is accomplished by applying electrical signals to at least one or more nerves using cutaneous, subcutaneous, implantable, or catheter-based neurostimulation assemblies, alone or in combination with one or more additional therapy or stimulation devices associated with the patient's heart, and/or with one or more therapeutic drug infusions or therapies, such as immune modulation therapy (IMT). | 2009-12-24 |
20090318987 | ISCHEMIA DETECTION FOR ANTI-ARRHYTHMIA THERAPY - An exemplary method includes detecting arrhythmia, detecting myocardial ischemia, determining whether the myocardial ischemia comprises local ischemia or global ischemia and, in response to the determining, calling for delivery of either a local ischemic anti-arrhythmia therapy or a global ischemic anti-arrhythmia therapy. Various other exemplary methods, devices, systems, etc., are also disclosed. | 2009-12-24 |
20090318988 | SIMPLIFIED BISPHASIC DEFIBRILLATOR CIRCUIT WITH MAKE-ONLY SWITCHING - A biphasic pulse delivery circuit for a defibrillator includes two capacitors, a first one of which is charged and delivers the first phase of the biphasic pulse and a second one of which is charged and delivers the second phase of the biphasic pulse. At least a portion of the charge on the second capacitor is provided by the current flow through the patient during delivery of the first pulse phase. Switches are provided for initiating the first phase, initiating the second phase, and terminating the second phase. In an illustrated circuit a shunt circuit path is provided to at least partially charge the second capacitor from the first capacitor prior to delivery of the second phase of the biphasic pulse. The inventive circuit can be controlled entirely with switching devices that only need to be closed during pulse delivery. | 2009-12-24 |
20090318989 | PACING CATHETER WITH STENT ELECTRODE - Cardioprotective pacing is applied to prevent and/or reduce cardiac injury associated with myocardial infarction (MI) and revascularization procedure. Pacing pulses are generated from a pacemaker and delivered through one or more pacing electrodes incorporated onto one or more percutaneous transluminal vascular intervention (PTVI) devices during the revascularization procedure. In one embodiment, at least one pacing electrode is constructed as, or incorporated onto, a stent at a distal end portion of a stent catheter. | 2009-12-24 |
20090318990 | PACING CATHETER WITH EXPANDABLE DISTAL END - Cardioprotective pacing is applied to prevent and/or reduce cardiac injury associated with myocardial infarction (MI) and revascularization procedure. Pacing pulses are generated from a pacemaker and delivered through one or more pacing electrodes incorporated onto one or more percutaneous transluminal vascular intervention (PTVI) devices during the revascularization procedure. In one embodiment, a PTVI device includes an expandable distal end to provide a stable electrical contact between a pacing electrode and the vascular wall of a blood vessel when the distal end is placed in the blood vessel. | 2009-12-24 |
20090318991 | PACING CATHETER FOR ACCESS TO MULTIPLE VESSELS - Cardioprotective pacing is applied to prevent and/or reduce cardiac injury associated with myocardial infarction (MI) and revascularization procedure. Pacing pulses are generated from a pacemaker and delivered through a plurality of pacing leads introduced into a patient's body through a percutaneous transluminal vascular intervention (PTVI) catheter have a plurality of exit ports. In one embodiment, the exit ports are arranged for the pacing leads to enter multiple specified blood vessels. | 2009-12-24 |
20090318992 | PACING CATHETER RELEASING CONDUCTIVE LIQUID - Cardioprotective pacing is applied to prevent and/or reduce cardiac injury associated with myocardial infarction (MI) and revascularization procedure. Pacing pulses are generated from a pacemaker and delivered through one or more pacing electrodes incorporated onto one or more percutaneous transluminal vascular intervention (PTVI) devices during the revascularization procedure. In one embodiment, a PTVI device releases a conductive liquid to provide a conductive medium between a pacing electrode and tissue of pacing site. | 2009-12-24 |
20090318993 | PACEMAKER INTEGRATED WITH VASCULAR INTERVENTION CATHETER - Cardioprotective pacing is applied to prevent and/or reduce cardiac injury associated with myocardial infarction (MI) and revascularization procedure. Pacing pulses are generated from a flexible pacemaker circuit integrated with a percutaneous transluminal vascular intervention (PTVI) device and delivered through pacing electrodes incorporated onto the PTVI device during the revascularization procedure. | 2009-12-24 |
20090318994 | TRANSVASCULAR BALLOON CATHETER WITH PACING ELECTRODES ON SHAFT - Cardioprotective pacing is applied to prevent and/or reduce cardiac injury associated with myocardial infarction (MI) and revascularization procedure. Pacing pulses are generated from a pacemaker and delivered through one or more pacing electrodes incorporated onto one or more percutaneous transluminal vascular intervention (PTVI) devices during the revascularization procedure. In one embodiment, at least one pacing electrode is incorporated onto the shaft of a PTVI device to allow the pacing pulses to be delivered to a site remote from an infarcted region where the distal end portion of the PTVI device is placed. | 2009-12-24 |
20090318995 | CARDIAC RESYNCHRONIZATION THERAPY OPTIMIZATION USING MECHANICAL DYSSYNCHRONY AND SHORTENING PARAMETERS FROM REALTIME ELECTRODE MOTION TRACKING - Therapy optimization includes tracking electrode motion using an electroanatomic mapping system and generating, based on tracked electrode motion, one or more mechanical dyssynchrony metrics to thereby guide a clinician in therapy optimization (e.g., via optimal electrode sites, optimal therapy parameters, etc.). Such a method may include a vector analysis of electrode motion with respect to factors such as times in cardiac cycle, phases of a cardiac cycle, and therapy conditions, e.g., pacing sites, pacing parameters and pacing or no pacing. Differences in position-with-respect-to-time data for electrodes may also be used to provide measurements of mechanical dyssynchrony. | 2009-12-24 |
20090318996 | OPTO-ELECTRICAL COHERENCE DETECTION OF HEMODYNAMICALLY COMPROMISING ARRHYTHMIA - System and methods for assessing sensed signals for determining a reliability measure of their accuracy with respect to a patient's true physiological status. As one example, the signals can include multiple, independently obtained signals, such as an electro-chemically based measure of cardiac activity and a plethysmography based measure of hemodynamic output which typically exhibit different morphologies and varying phase shifts with respect to each other. One manner of assessing the signals is to transform them into the frequency domain, such as via a Fast Fourier Transform (FFT), and evaluate them, such as by a coherence determination, to determine the degree of their mutual agreement. This can be used to assess the reliability of the sensing. Therapy can be delivered under certain observed conditions, such as a condition of hemodynamic insufficiency where anti-tachycardia pacing and/or shocking therapy can be delivered. | 2009-12-24 |
20090318997 | System and Method of Detecting and Diagnosing Pacing System Malfunctions - A method of diagnosing a malfunction of a pacing system includes the steps of receiving a biopotential signal, detecting a pacing system malfunction, detecting a cause of the malfunction, and displaying the detected malfunction and detected cause of the malfunction. A pacing system is also disclosed herein. The system includes an electrode array that receives a biopotential signal associated with the pacing system. A malfunction detector applies a malfunction logic to the biopotential signal to identify a pacing system malfunction and applies a morphology logic to the biopotential signal to identify a morphology of the biopotential signal. An output generator receives an indication of the identified pacing system malfunction and the identified cause of the malfunction and creates an output indicative of the identified pacing system malfunction and the identified cause. | 2009-12-24 |
20090318998 | CONFIGURATION AND METHOD FOR THE MANAGEMENT OF DATA OF A PLURALITY OF PROGRAMMABLE PERSONAL MEDICAL DEVICES - The invention relates to a configuration and a method for the management of data of a plurality of programmable personal medical devices. The configuration comprises a first plurality of personal devices, a second plurality of patient devices each calibrated to at least one personal device, a third plurality of programming devices each calibrated to at least one personal device, a central management unit, a service center, and a management database. The patient devices and/or the programming devices are controlled using management data, upon establishment of the existence of a communication between the management unit and the patient device and/or a programming device, on the basis of this establishment and on the basis of stored management data, specific management data being transmitted to the patient device and/or programming device. | 2009-12-24 |
20090318999 | METHODS AND DEVICES FOR JOINING CABLES - Methods for ultrasonically joining portions of a medical lead are provided. One method includes providing a conductor, a fitting and a coil electrode. The conductor has a distal portion that includes an inner conductive portion and an outer insulative portion. The fitting has a first cavity and a second cavity, the first cavity being sized and configured to receive the distal portion of the conductor and the second cavity being sized and configured to receive a portion of the coil electrode. The conductor is ultrasonically welded within the first opening, providing a mechanical and electrical attachment. The coil electrode is also electrically coupled to the fitting, providing an electrical pathway from the conductor to the coil electrode. Also provided are medical leads including ultrasonic bonds and other methods of ultrasonically joining portions of a medical lead. | 2009-12-24 |
20090319000 | METHODS AND APPARATUS FOR EFFECTUATING A CHANGE IN A NEURAL-FUNCTION OF A PATIENT - The present disclosure is directed generally to methods and apparatus for effectuating a change in a neural function of a patient. A method in accordance with a particular embodiment includes implanting an electrode at a cortical stimulation site selected to promote recovery of the affected neural-function, with the cortical stimulation site being at least proximate to the cortex. The method can further include estimating a threshold for the specific patient at which an electrical signal delivered via the implanted electrode directly triggers a neural reaction associated with the stimulation site in response to the delivered electrical signal, and electrically stimulating the cortical stimulation site by Passing an electrical current through the electrode. | 2009-12-24 |
20090319001 | FEEDBACK METHOD FOR DEEP BRAIN STIMULATION WITH DETECTION OF GENERALIZED EFFERENCE COPY SIGNALS - Disclosed is a method for improving cognitive function or for improving coordination of function across a patient's cortical regions. The method includes applying electrical stimulation to at least a portion of the patient's subcortical structures involved in the generation and control of generalized efference copy signals. Internally generated movement of the patient is then detected and, in response to such internally generated movement, application of electrical stimulation is controlled. The method of the present invention has a number of benefits, including increasing flexibility in identifying targets for stimulation, improving the probability of successfully treating brain injury, and permitting patient biofeedback and self-regulation. | 2009-12-24 |
20090319002 | METHODS AND APPARATUS FOR TRANSCRANIAL STIMULATION - The present invention provides systems, apparatus and methods for applying electric current to neurons in the brain to treat disorders and to improve motor and/or memory functions in a patient. In a method according to the invention, an electrode is positioned adjacent to and spaced from the skin surface of the patient's head and an electric current is applied through the electrode to a target region in the brain to modulate one or more neurons in the target region. The electrode is housed within an enclosure and spaced from the skin surface so that the electrode does not directly contact the patient's tissue, which reduces the potential for collateral tissue damage or necrosis and shields the electrode from the patient's tissue which substantially inhibits Faradic products (e.g., H | 2009-12-24 |
20090319003 | Electrical Stimulation Method for Reduction of Joint Compression - An electrical stimulation method for the reduction of joint compression is disclosed. In a preferred embodiment, the method utilizes an electrical stimulation device that includes a plurality of channels of electrodes each of which includes at least a first and second electrode positioned in electrical contact with tissue of at least two muscles crossing a joint. Agonist/antagonist muscles involved in abduction/adduction, flexion/extension, supination/pronation, protraction/retraction, and/or eversion/inversion of body regions via joint movement are stimulated with a patterned series of electrical pulses through channels of electrodes in accordance with a procedure for reducing joint compression. The patterned series of electrical pulses may comprise: a plurality of cycles of a biphasic sequential pulse train pattern; a plurality of cycles of a biphasic overlapping pulse train pattern; a plurality of cycles of a triphasic sequential pulse train pattern; and a plurality of cycles of a triphasic overlapping pulse train pattern. | 2009-12-24 |
20090319004 | APPARATUS AND METHOD FOR STIMULATING A BRAIN OF A PERSON - An apparatus for stimulating a brain ( | 2009-12-24 |
20090319005 | STOCHASTIC STIMULATION IN A HEARING PROSTHESIS - A hearing prosthesis configured for delivery of stochastic stimulation to a recipient. The hearing prosthesis comprises a sound pickup component configured to receive a sound signal having at least one pitch; a stochastic stimulation generator configured to generate a stochastic sequence of stimulation pulses having first and second inter-pulse intervals distributed stochastically throughout the sequence within controlled limits, the first inter-pulse interval based on the at least one pitch; and at least one stimulation channel to deliver the sequence of electrical stimulation pulses to the recipient. | 2009-12-24 |
20090319006 | IMPLANTABLE TRANSDUCER DEVICES - Receiver-stimulators comprise a nearly isotropic transducer assembly, demodulator circuitry, and at least two tissue contacting electrodes. Use of near isotropic transducers allows the devices to be implanted with less concern regarding the orientation relative to an acoustic energy source. Transducers or transducer elements having relatively small sizes, typically less than ½ the wavelength of the acoustic source, enhance isotropy. The use of single crystal piezoelectric materials enhance sensitivity. | 2009-12-24 |
20090319007 | Shocking device having a time-based monitoring and recording circuit - An electronic shocking device comprising a voltage drop detector which signals an integrated circuit to record the occurrence of a shock when the device voltage drops within a preset tolerance corresponding to a recommended level of shocking current. The voltage drop detector or integrated circuit may also activate a display to signal the device operator that the device is actually shocking a subject. | 2009-12-24 |
20090319008 | PROBE DEVICE, SYSTEM AND METHOD FOR PHOTOBIOMODULATION OF TISSUE LINING A BODY CAVITY | 2009-12-24 |
20090319009 | DEVICE FOR PREDICTING A BODY TEMPERATURE OF A PATIENT | 2009-12-24 |
20090319010 | Body Heating Device - To realize a body surrounding solenoid-type body heating device with small coil impedance which can generate a magnetic flux of predetermined density to one part of the living body near the affected area in the solenoid coil, a body heating device | 2009-12-24 |
20090319011 | METHOD AND SYSTEM FOR WARMING OR COOLING A FLUID - The invention is directed generally to a method and system for controlling the temperature of a fluid, i.e., warming or cooling a fluid, and more particularly, to a method and system for warming a fluid to be delivered to the body of a patient. In a preferred embodiment, a method and system for warming a fluid to be delivered into the body of a patient is provided and may include a controller and a fluid delivery-line. | 2009-12-24 |
20090319012 | MODULAR STIMULATION LEAD NETWORK - A medical kit and method for treating an ailment, such as chronic pain is provided. The kit comprises first and second medical leads, e.g., stimulation leads. Each lead comprises an elongated body and at least one operative element. The first medical lead comprises a coupling mechanism, such as a slot, and the second medical lead comprises a complementary mechanism, such as a rail, that slidably engages the coupling mechanism of the first medical lead. The method may comprise delivering the first medical lead into a patient's body, e.g., into the epidural space of the patient, and delivering the second medical lead into the patient's body by sliding the complementary coupling mechanism of the second medical lead along the coupling mechanism of the first medical lead. | 2009-12-24 |
20090319013 | IMPLANTABLE NEURAL STIMULATION ELECTRODE ASSEMBLIES AND METHODS FOR STIMULATING SPINAL NEURAL SITES - An implantable neurostimulation electrode assembly comprises a first electrode unit and a second electrode unit configured to be arranged in a side-by-side configuration. The first electrode unit includes a dielectric first paddle, a plurality of first electrodes carried by the first paddle, and a guideline. The guideline has a distal section affixed to the first paddle and a proximal section having a length configured to extend externally of a patient. The second electrode unit has a dielectric second paddle and a plurality of second electrodes carried by the second paddle. The second paddle is configured to travel along the guideline and contact the first paddle in the side-by-side configuration. As a result, the first and second electrode units of this embodiment can be passed percutaneously through the same percutaneous entry hole and assembled in vivo at the stimulation site to form a larger paddle-type electrode array without surgical implantation. | 2009-12-24 |
20090319014 | LEAD ASSEMBLY AND RELATED METHODS - Defibrillator lead designs and methods for manufacturing a lead including a fibrosis-limiting material covering, a shocking coil electrode, and an implantable lead body are disclosed herein. The fibrosis limiting material includes one or more passages therein and bonding material, such as medical adhesive, is disposed over and under a portion of the coating and within the passage. | 2009-12-24 |
20090319015 | EXPANDABLE ASSEMBLY FOR CARDIAC LEAD FIXATION - A cardiac lead includes a lead body that defines a passage, a conductive element that extends through the passage, and a fixation assembly. The fixation assembly includes a threaded member threadably engaged with the conductive element such that rotation of the threaded member causes the threaded member to translate longitudinally relative to the conductive element. A fixation element has a first end coupled to the threaded member and a second end coupled to a fixed location. A resilient membrane extends over the fixation element such that rotation of the threaded member affects the resilient membrane radially with respect to the conductive element. | 2009-12-24 |
20090319016 | PROCESS FOR PRODUCTION OF POROUS BODY AND USES THEREOF - A process for producing a porous body with different physical properties in desired regions is provided by pore forming treatment, not by bonding two or more materials made porous beforehand, with, for example, an adhesive. Raw materials are prepared, each of which contains a polymer and a raw material preparation solvent. At least two types of the raw materials having different compositions are prepared. Thereafter, the respective raw materials are frozen into desired shapes to form frozen bodies thereof. The frozen bodies thus formed are brought into contact with each other to form an assembly thereof, the assembly is exposed to a condition under which the frozen bodies begin to melt, and the assembly is then freeze-dried. Thus, a porous body having regions different in physical properties can be obtained. Such a porous body can be used as, for example, an adhesion inhibitory material or a scaffold for a cell culture. | 2009-12-24 |
20090319017 | VASCULAR STENTING FOR ANEURYSMS - Described herein are flexible implantable occluding devices that can, for example, navigate the tortuous vessels of the neurovasculature. The occluding devices can also conform to the shape of the tortuous vessels of the vasculature. In some embodiments, the occluding devices can direct blood flow within a vessel away from an aneurysm or limit blood flow to the aneurysm. Some embodiments describe methods and apparatus for adjusting, along a length of the device, the porosity of the occluding device. In some embodiments, the occluding devices allows adequate blood flow to be provided to adjacent structures such that those structures, whether they are branch vessels or oxygen-demanding tissues, are not deprived of the necessary blood flow. | 2009-12-24 |
20090319018 | DELIVERY SYSTEM FOR A MEDICAL DEVICE AND METHOD FOR OPERATING A DELIVERY SYSTEM FOR A MEDICAL DEVICE - The invention relates to a delivery system for a medical device and a method for operating a delivery system for a medical device, in particular a stent having a proximal end and a distal end, an inner shaft enclosing an inner lumen and an outer shaft surrounding the inner shaft in at least some areas and enclosing an intermediate lumen. One or more openings are provided in the inner shaft establishing a fluid connection between the inner lumen and the intermediate lumen. | 2009-12-24 |
20090319019 | Expandable Tip Delivery System For Endoluminal Prosthesis - An improved delivery system for an implantable medical device includes a retention sheath for an implantable medical device. The retention sheath includes a central lumen extending from a proximal end to a distal end of the retention sheath, and a tapered portion disposed at a distal end of the retention sheath. The tapered portion of the retention sheath includes a first layer made of a low-friction material. The first layer may be movable from a compressed, folded configuration in an initial position, to a substantially uncompressed and unfolded configuration in a deployment position. The retention sheath also includes a second layer made of an expandable material. The second layer is disposed radially outward of and in contact with the first layer, and the second layer is configured to expand in a substantially radially outward direction when the first layer moves from the initial position to the deployment position. | 2009-12-24 |
20090319020 | DEVICES, SYSTEMS, AND METHODS FOR PROMOTING ENDOTHELIALIZATION - Devices, systems, and methods for promoting endothelialization and preventing restenosis are disclosed. At least some of the embodiments disclosed herein promote endothelialization and prevent restenosis by reducing local blood flow turbulence. At least some of the embodiments disclosed herein promote endothelialization and prevent restenosis by directing endothelial progenitor cells to a targeted site using magnetic and other means. | 2009-12-24 |
20090319021 | BIFURCATED MEDICAL APPLIANCE DELIVERY APPARATUS AND METHOD - The present invention, in preferred embodiments, provides delivery and deployment apparatuses for bifurcated stents capable of comfortably cradling the corina of bifurcated target tissue between the arms of the bifurcated stent as each arm of the bifurcated stent is delivered to a respective side branch. In particular, a family of apparatuses is provided that may be indicated for vascular and non-vascular intervention. | 2009-12-24 |
20090319022 | STENT GRAFT - A stent graft ( | 2009-12-24 |
20090319023 | Stents and Stent Grafts - The subjected devices include a stent, a graft and a means for attaching the graft to the stent. One or more members are received in a permanent or temporary receptacle within the stent attach the graft to the stent. In one variation, an interference fit is employed; in another, the graft is bonded to a stent-captured member(s). | 2009-12-24 |
20090319024 | REMOVABLE STENT AND METHOD OF MANUFACTURE THEREOF - A removable stent may include, for example, an extension or protrusion, or a cut or angled end, which may be easily grasped for removal by for example forceps. A stent may be molded to form such graspable extensions, or may be cut and/or melted or otherwise deformed as part of manufacture. | 2009-12-24 |
20090319025 | RESONATOR FOR MEDICAL DEVICE - A device resonator for medical device is provided. The resonator device includes a helical structure and a capacitor structure. The resonator device can be used in conjunction with a medical device, including a stent. | 2009-12-24 |
20090319026 | Composite Stent with Reservoirs for Drug Delivery and Methods of Manufacturing - A composite stent structure and methods of manufacturing same, include a stent wall having two or more layers of the same or different material. The wall provides various means of drug delivery while maintaining the stent's overall structure. The outer layers and/or inner layers may have holes, reservoirs, or openings that allow for the delivery of drugs or other therapeutic agents. | 2009-12-24 |
20090319027 | SELF-EXPANDABLE STENT - A self-expandable stent includes axially arranged wavy-line annular bodies having a first shared linear portion and a second shared linear portion on one end side, a third shared linear portion and a fourth shared linear portion on the other end side, a first bent linear portion coupled with the first and third shared linear portions, a second bent linear portion coupled with the third and second shared linear portions, a third bent linear portion coupled with the second and fourth shared linear portions, and a fourth bent linear portion coupled with the fourth and first shared linear portions. Two of the four bent linear portions have a first equal number of bends and a common form at inversion, and the other two of the four bent linear portions have an equal number of bends different from the first equal number of bends and a common form at inversion. | 2009-12-24 |
20090319028 | STENT FABRICATION VIA TUBULAR CASTING PROCESSES - Tubular casting processes, such as dip-coating, may be used to form substrates from polymeric solutions which may be used to fabricate implantable devices such as stents. The polymeric substrates may have multiple layers which retain the inherent properties of their starting materials and which are sufficiently ductile to prevent brittle fracture. Parameters such as the number of times the mandrel is immersed, the duration of time of each immersion within the solution, as well as the delay time between each immersion or the drying or curing time between dips and withdrawal rates of the mandrel from the solution may each be controlled to result in the desired mechanical characteristics. Additional post-processing may also be utilized to further increase strength of the substrate or to alter its shape. | 2009-12-24 |
20090319029 | DOCKING APPARATUS AND METHODS OF USE - A system for treating an aneurysm in a blood vessel comprises a docking scaffold having with upstream and downstream ends, and a central passageway therebetween. The upstream end engages the blood vessel upstream of the aneurysm. A portion of a first and second scaffolds are slidably received in the central passageway such that an outside surface of the first and second scaffolds engage an inside surface of the docking scaffold. A double-walled filling structure has outer and inner walls and the filling structure is adapted to be filled with a hardenable fluid filling medium so that the outer wall conforms to an inside surface of the aneurysm and the inner wall forms a substantially tubular lumen to provide a path for blood flow therethrough. The double-walled filling structure is coupled with at least one of the first and second leg scaffolds in expanded configuration. | 2009-12-24 |
20090319030 | Stent with Protruding Branch Portion for Bifurcated Vessels - The present invention is directed to a stent for use in a bifurcated body lumen having a main branch and a side branch. The stent comprises a radially expandable generally tubular stent body having proximal and distal opposing ends with a body wall having a surface extending therebetween. The surface has a geometrical configuration defining a first pattern, and the first pattern has first pattern struts and connectors arranged in a predetermined configuration. The stent also comprises a branch portion comprised of a second pattern, wherein the branch portion is at least partially detachable from the stent body. | 2009-12-24 |
20090319031 | Bioabsorbable Polymeric Stent With Improved Structural And Molecular Weight Integrity - Various embodiments of the present invention include implantable medical devices such as stents manufactured from polymers, and more particularly, biodegradable polymers including biodegradable polyesters. Other embodiments include methods of fabricating implantable medical devices from polymers. The devices and methods utilize one or more stabilizers, where each stabilizer may be chosen from the following categories: free radical scavengers, peroxide decomposers, catalyst deactivators, water scavengers, and metal scavengers. | 2009-12-24 |
20090319032 | ENDOPROSTHESIS COATING - An endoprosthesis, e.g., a stent (e.g., a drug eluting stent), that includes a porous surface and hollow elements integrated with a coating on the surface and a method of making the same are disclosed. | 2009-12-24 |
20090319033 | METHOD FOR ENDOTHELIAL CELL EXTRACTION FROM ADISPOSE TISSUES - Adipose tissue has proven to serve as an abundant, accessible, and rich source of endothelial or vascular endothelial cells suitable for tissue engineering. We describe a detailed method for the isolation and purification of endothelial cells using purified enzymes and antibody-based selection. The cells can be obtained from liposuction procedures and used in vascular grafts. | 2009-12-24 |
20090319034 | METHOD OF DENSIFYING ePTFE TUBE - The present invention relates to a prosthetic structure, including a densified layer of expanded polytetrafluoroethylene (ePTFE) and a method for manufacturing the same. The invention includes the steps of providing a layer of ePTFE, desirably a tubular layer; applying the layer of ePTFE to a mandrel; mechanically compressing the layer of ePTFE on the mandrel; and removing the compressed ePTFE; where the compressed ePTFE is denser than uncompressed ePTFE. The compressed ePTFE has a water entry pressure (WEP) value of at least 15 psi, and desirably a WEP of at least about 20 psi. | 2009-12-24 |
20090319035 | ANTIMICROBIAL COATING - Described herein are coatings containing water-soluble oligodynamic metal salts that are formulated and applied from hydrophobic solvents. In particular, articles of manufacture comprising polymer coatings containing oligodynamic metal salts can include hydrophobic polymer coatings made from water-reactive monomers and hydrophilic polymers compounded in hydrophobic solvents which contain a small amount of water that aids in the solubilization and suspension of the oligodynamic metal salts. Methods of preparing these antimicrobial polymer coatings, and methods of coating a substrate to produce an article of manufacture having an antimicrobial polymer coating are also described. | 2009-12-24 |
20090319036 | Medical Devices Made From Polymers With End Group Modification For Improved Thermal Stability - Implantable medical devices and methods of forming thereof made from polymers with end groups providing improved thermal stability are disclosed. Implantable medical devices made from such polymers including stabilizing agents are additionally disclosed. | 2009-12-24 |
20090319037 | RETAINING MECHANISMS FOR PROSTHETIC VALVES - Disclosed herein are representative embodiments of methods, apparatus, and systems used to deliver a prosthetic heart valve to a deficient valve. In one embodiment, for instance, a support stent is delivered to a position on the surface of the outflow side of a native heart valve of a patient, the support stent defining a support-stent interior. An expandable prosthetic heart valve is delivered into the native heart valve from the inflow side of the native heart valve and into the support-stent interior. The expandable prosthetic heart valve is expanded while the expandable prosthetic valve is in the support-stent interior and while the support stent is at the position on the surface of the outflow side of the heart valve, thereby causing one or more of the native leaflets of the native heart valve to be frictionally secured between the support stent and the expanded prosthetic heart valve. | 2009-12-24 |
20090319038 | CONNECTION SYSTEMS FOR TWO PIECE PROSTHETIC HEART VALVE ASSEMBLIES AND METHODS FOR MAKING AND USING THEM - A heart valve assembly includes a prosthesis and a prosthetic valve to replace a preexisting natural or prosthetic heart valve within a biological annulus. The prosthesis includes an annular member, a flexible core at least partially defining a sewing cuff extending radially outwardly from the annular member, a rail ring disposed between the flexible core and the annular member, and a plurality of guide rails extending from the rail ring through respective openings in the flexible core. A fabric covering covers the prosthesis, and the guide rails extend through respective openings in the fabric covering. The prosthetic valve includes a frame including receptacles for receiving respective guide rails. After implanting the prosthesis within a biological annulus, the prosthetic valve is advanced along the guide rails until retention elements on the guide rails engage the receptacles to secure the prosthetic valve relative to the prosthesis. | 2009-12-24 |
20090319039 | Method in Eye Surgery - A method for prevention of migration of epithelial cells in a capsular bag of an eye of a mammal is provided. The method comprises removing the natural lens of the eye from the capsular bag; introducing an object with at least one sharp edge into the capsular bag, in such a way that said sharp edge contacts the inside of the capsular bag to form a barrier preventing migration of epithelial cells across said barrier; and injecting a lens-forming composition into the capsular bag. | 2009-12-24 |
20090319040 | ACCOMMODATIVE INTRA-OCULAR LENS - An accommodative intra-ocular lens deformable between the unaccommodating and accommodating configurations upon the relaxation and contraction of the ciliary muscle. The lens anterior and posterior portions are substantially sealingly joined together about their peripheral edges and define a lens internal volume filled with a substantially incompressible lens internal fluid. Causing a variable internal fluid pressure exerted on the lens inner surfaces. The lens is configured such that radius of curvature of both the central and peripheral sections of the lens anterior portion will decrease upon an increase in internal fluid pressure and increase upon a decrease in internal fluid pressure. | 2009-12-24 |
20090319041 | HIGHLY HAEMOCOMPATIBLE AND BIODEGRADABLE POLYMER AND USES THEREOF - A new biodegradable polymer composed by poly(D,L)lactic acid (PDLLA) and Vitamin E (α-tocopherol) is disclosedα. This polymer shows a high degree of haemocompatibility compared to the original polymer (PDLLA) and is a good candidate as coating material of different biomaterials. | 2009-12-24 |
20090319042 | THREADED PART THAT IS TO BE CONNECTED TO THE THREADED HOLE OF AN IMPLANT - Threaded part ( | 2009-12-24 |
20090319043 | HELICOIL INTERFERENCE FIXATION SYSTEM FOR ATTACHING A GRAFT LIGAMENT TO A BONE - A helicoil interference fixation system comprising:
| 2009-12-24 |
20090319044 | Methods and Compositions for Improving the Incorporation of Orthopaedic and Orthodontic Implants - The present invention provides methods of improving the incorporation of an implantable device into a bone of a host in need thereof. More particularly, the methods of the present invention include implanting the device into the bone of a host, wherein the device is at least partially made of a non-metallic material. Disposed on at least one surface of the device is an amount of hydroxyapatite and bisphosphonate, which in combination, are effective to reduce osteolysis and improve incorporation of the implant into the host bone compared to an implant without the hydroxyapatite and/or bisphosphonate. The present invention also provides methods for making such implants, as well as, the implants themselves. | 2009-12-24 |
20090319045 | Cancellous constructs, cartilage particles and combinations of cancellous constructs and cartilage particles - Constructs that are at least partially constructed of allograft cancellous bone are disclosed, along with cartilage particles that may be used with the constructs for repairing articular cartilage defects. A multi-piece construct includes a base member, a cap member and at least one pin that secures the cap member to the base member. The base member may be constructed of mineralized cancellous bone, and is used to replace the subchondral bone removed when a surgeon cuts a bore in the area of an adjacent cartilage defect. The base member includes a blind bore and first and second through-going transverse bores in opposite sides of a wall of the base member. The cap member includes an upper section that has a thickness that is similar to that of a patient's surrounding articular cartilage layer and a stem depending from the upper section that is dimensioned to be received in and by the blind bore of the base member. The stem includes a transverse through-going bore, which may be aligned with the transverse through-going bores of the base member to receive the pin therein when the construct has been assembled. The cap member is at least partially formed of demineralized allograft cancellous bone, into which a mixture containing lyophilized, freeze-milled allograft cartilage particles may be infused for the repair of articular cartilage defects. The cartilage particles have a size within a range of from about 10 microns to about 210 microns. | 2009-12-24 |
20090319046 | HYOID SUSPENSION FOR OBSTRUCTIVE SLEEP APNEA - In an improved method for surgically treating a sleep-related breathing disorder, comprising hyoid distruction/expansion and hyo-mandibular suspension, an implant comprises a polypropylene and/or reticulated elastomeric biostable polyurethane matrix. The matrix is positioned between two or more segments of the distructed hyoid bone. A single or multiple midline or paramedian incisions are made under a patient's chin; soft tissues overlying the mandible are cleaned; a first screw is inserted into the edge of the mandible; a second screw is inserted into the inferior edge of the mandible; a second horizontal incision is made over the body of the hyoid; the infrahyoid muscles are separated from the body of the hyoid bone; the hyoid is refracted and stabilized; the sternohyoid and thyrohyoid muscles are detached from the body of the hyoid between the lesser cornuae; the hyoid bone is divided midline or paramedian into two or more segments; and an absorbable or nonabsorbable, rigid or semirigid, implant is positioned between segments of the hyoid bone. The hyoid bone is stabilized by the implant; and sutures or portions of polypropylene and/or polyurethane matrix are passed around the hyoid bone segments and implant to connect to muscle still attached to the upper portion of the hyoid bone, wherein the hypopharyngeal airway is expanded. | 2009-12-24 |
20090319047 | RECESS-RAMP KNEE JOINT PROSTHESIS - A recess-ramp knee joint prosthesis comprising a femoral and a tibial component is configured to reproduce normal kinematics and function. Asymmetric condular surfaces and a cupola of the femoral component interact with corresponding dished surfaces and a ramp of the tibia thereby duplicating the behavior of the anatomical knee. | 2009-12-24 |
20090319048 | Total Knee Replacement Prosthesis - A knee replacement prosthesis comprising a femoral component and a tibial component that enable anterior-posterior translation of the femur relative to the tibia and enable the tibia to rotate about its longitudinal axis during flexion of the knee. The femoral component connects to the distal end of a resected femur and includes medial and lateral condyles having distal, articulating surfaces, and a patellar flange having a patellar articulating surface. The tibial component connects to the proximal end of a resected tibia and includes a proximal bearing surface with medial and lateral concavities that articulate with the medial and lateral condyles. The articulating surfaces of the condyles and concavities are defined by sections of toroids. | 2009-12-24 |
20090319049 | Total Knee Replacement Prosthesis With High Order NURBS Surfaces - A knee replacement prosthesis comprising a femoral component and a tibial component that enable anterior-posterior translation of the femur relative to the tibia and enable the tibia to rotate about its longitudinal axis during flexion of the knee. The femoral component connects to the distal end of a resected femur and includes medial and lateral condyles having distal, articulating surfaces, and a patellar flange having a patellar articulating surface. The tibial component connects to the proximal end of a resected tibia and includes a proximal bearing surface with medial and lateral concavities that articulate with the medial and lateral condyles. The condylar articulating surfaces and the said concavities are substantially defined by non-uniform, rational B-spline surfaces (NURBS). | 2009-12-24 |
20090319050 | Method and Apparatus for Wrist Arthroplasty - A wrist prosthesis system to replace at least a portion of a bone of a wrist of a patient. The system includes a carpal implant to replace at least a portion of a carpal bone of a carpal complex of the patient. The carpal implant includes a base and an augment that replaces at least a portion of the carpal bone. The augment is removably coupled to the base. | 2009-12-24 |