| 45th week of 2012 patent applcation highlights part 48 |
| Patent application number | Title | Published |
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| 20120283663 | Sheath for Protection of Medical Devices and Method of Use Thereof - A protective sheath for protecting elongated medical devices positioned in, or through, the sheath while performing a surgical procedure. The sheath is formed of a thin, flexible material that provides and maintains a clean and sterile and reliable path for medical instruments to travel within. The device provides a barrier between a medical instrument, the orifice/opening in which the instrument enters the human body, and the path these instruments travel to other body organs or locations, and reduces unwanted translocation. | 2012-11-08 |
| 20120283664 | Use of Polyoxyalkylene Diamine-Based Polyguanidine Derivatives for Medical Articles - The invention relates to the use of at least one polymeric guanidine derivative having a biocidal effect, which can be obtained by polycondensating a guanidine acid addition salt with an amine mixture containing at least one diamine, which is selected from the group consisting of alkylene diamine and oxyalkylene diamine, as an additive in a composition for medical articles. | 2012-11-08 |
| 20120283665 | METHOD FOR COATING INNER SURFACE OF MEDICAL TUBE MADE FROM VINYL CHLORIDE WITH ANTI-THROMBOTIC MATERIAL - The present invention provides a method for coating an inner surface of a polyvinyl chloride medical tube containing a plasticizer with an antithrombogenic material composed of a specific (meth)acrylate copolymer. The simple method of the present invention is capable of evenly and efficiently coating an inner surface of a polyvinyl chloride medical tube with a sufficient amount of an antithrombogenic material without causing appearance deterioration or uneven coating due to elution of the plasticizer. The method is performed by passing through a tube a solution that is prepared by dissolving an antithrombogenic material in a solvent composed of water and at least one alcohol that is adjusted to dissolve the copolymer of the antithrombogenic material but does not dissolve the plasticizer, then subsequently passing water through the tube, and finally drying the tube. | 2012-11-08 |
| 20120283666 | DRUG ELUTING COCHLEAR IMPLANTS - Drug delivery systems and biocompatible coatings for use with implantable stimulation devices such as cochlear implants have been developed. These drug delivery systems and coatings comprise polyhydroxyalkanoate (PHA) polymers and copolymers. The drug delivery systems may be used to deliver pharmacologically active substances, for example, directly from a cochlear implant to the inner ear. The coatings can impart lubricity to cochlear devices for ease of insertion of the electrodes. In the preferred embodiment, the drug delivery system comprises a polyhydroxyalkanoate polymer, and in the most preferred embodiment, the PHA polymer comprises poly(4-hydroxybutyrate) (P(4HB)) or copolymer thereof. A particularly preferred embodiment is where the silicone sheath of the cochlear implant electrodes has been surface modified, and coated with P(4HB), and the P(4HB) either contains a pharmacologically active substance or has been coated with such a substance. | 2012-11-08 |
| 20120283667 | Medical Lumen Access Device Assembly Including Medical Lumen Access Device Holder And Method of Use - A medical lumen access device assembly includes a medical lumen access device holder including an elongate tube defining a lumen extending from a proximal opening of the elongate tube to a distal opening of the elongate tube. A check valve is positioned over an opening of the elongate tube and includes a valve member having a biased closed position wherein an internal volume defined by the lumen is fluidly blocked from an exterior of the elongate tube at the opening and an open position defining a fluid path from the exterior to the internal volume through the opening. The medical lumen access device assembly also includes a medical lumen access device disposed at least partially within the lumen and having a proximal segment extending beyond the distal opening. At least a portion of the medical lumen access device includes a hydrophilic coating. | 2012-11-08 |
| 20120283668 | APPARATUS AND METHOD FOR USING EFFERVESCENT TABLETS FOR COSMETIC CARE - An apparatus and method for providing cosmetic treatment to skin comprise one material chemically active in a solid form preferably in a tablet form and a second material which is chemically reactive with the first material so that effervescence is produced during the reaction. The chemically active materials may be activated by a user for providing cosmetic treatment to skin. The activation releases effervescence which urges granules of the reacting materials onto the skin. The size of the granules lowers during the reaction thus providing continuously refining peeling to the skin. | 2012-11-08 |
| 20120283669 | PUNCTAL PLUGS FOR CONTROLLED RELEASE OF THERAPEUTIC AGENTS - Lacrimal inserts such as punctal plugs may be utilized for delivery of medication to the eye. The plug includes a body portion sized to pass through a lacrimal punctum and be positioned within a lacrimal canaliculus of the eyelid. The plug may contain a core, or reservoir, at least partially within the body portion comprising a therapeutic agent that is configured for controlled, pulsatile release into the eye. | 2012-11-08 |
| 20120283670 | PERCUTANEOUS ABSORPTION PREPARATION COMPRISING ANTI-DEMENTIA DRUG - The present invention relates to a percutaneous absorption preparation comprising an anti-dementia drug, which is lower skin irritation. More specifically, the present invention relates to a percutaneous absorption preparation comprising a drug-containing layer comprising an anti-dementia drug, a polymer compound having an amino group, a polyhydric alcohol fatty acid ester, a polyhydric alcohol, a polyvalent carboxylate ester, and a styrenic polymer compound, wherein the content of the anti-dementia drug is 0.5-20 mass % of the drug-containing layer. | 2012-11-08 |
| 20120283671 | ANTI-INFLAMMATORY ANALGESIC ADHESIVE PATCH FOR EXTERNAL USE - An external patch containing diclofenac hydroxyethylpyrrolidine prepared by laminating an adhesive layer on a backing, wherein said adhesive layer is characterized by comprising 5-50% by weight of styrene•isoprene•styrene block copolymer, 20-50% by weight of a tackifier resin, 5-70% by weight of a softening agent, and 0.5-20% by weight of one or more solubilizers selected from N-methyl-2-pyrrolidone, propylene glycol and dimethyl sulfoxide as essential ingredients, and 0.5-20% by weight of diclofenac hydroxyethylpyrrolidine as an active ingredient. The patch has excellent transdermal absorption, less skin-irritation and excellent stability of the drug. | 2012-11-08 |
| 20120283672 | METHOD AND APPARATUS FOR WOUND TREATMENT - A wound treatment device comprises a polyurethane or polyether foam pad, adapted for insertion substantially within a wound cavity; a pump for supplying fluid flow to the wound site; and a collection canister for receiving wound fluids drawn from the wound cavity. The foam pad, pump and collection canister are in fluid communication with one another through a single hospital grade hose having a plurality of tiny apertures in the portion that is central to the foam pad. These apertures are adapted to allow fluids from the wound cavity to be drawn into the flow from the pump to the canister according to Bernoulli's theorem. | 2012-11-08 |
| 20120283673 | KIT FOR PREDICTING IMPLANTATION SUCCESS IN ASSISTED FERTILIZATION - A kit for determining for a female subject the implantation potential of embryos obtained or to be obtained by assisted fertilization is described. The kit includes at least one reagent suitable for detection of levels of FF G-CSF or FF G-CSF mRNA, such as anti-G-CSF antibody or a nucleic acid probe for detection of levels of G-CSF mRNA. The kit may also include a set of concentration standards of FF G-CSF and aspirator tips for removing an oocyte and follicular fluid. | 2012-11-08 |
| 20120283674 | SYSTEMS AND METHODS FOR CONTROLLING INFLAMMATORY RESPONSE - A method and system for controlling inflammatory response at an internal tissue site of a patient utilizes a reduced-pressure treatment device. Controlling the inflammatory response may be accomplished in a number of ways that involve treating the inflammatory milieu. Treating the inflammatory milieu may include removing or moderating pro-inflammatory stimuli, e.g., fluids, enhancing perfusion of the tissue at or near the internal tissue site, or providing reduced-pressure therapy. The reduced-pressure treatment device is placed at or near the internal tissue site and is fluidly coupled to an external reduced-pressure source. The reduced-pressure treatment device provides reduced pressure proximate the tissue site and treats the inflammatory milieu. The reduced-pressure treatment device for controlling inflammatory response may be a minimally-invasive treatment device. | 2012-11-08 |
| 20120283675 | SYSTEM FOR PROVIDING FLUID FLOW TO NERVE TISSUES - Provided is an apparatus that includes a nerve conduit, a manifold and a support structure for providing a reduced pressure. Also provided is a system that includes a source of reduced pressure, a nerve conduit, a manifold, a support structure and a conduit for providing fluid communication between the manifold support and the source of reduced pressure. Additionally provided is a method that includes implanting the above nerve conduit, manifold and support structure at a site of damaged nerve tissue and applying a reduced pressure to the manifold thereby stimulating repair or regrowth of nerve tissue. | 2012-11-08 |
| 20120283676 | METHOD OF CONTROLLING THE FLOW OF BODILY FLUID - A system and method are disclosed for automatically limiting the drainage of a bodily fluid such as cerebrospinal fluid (CSF) from a patient into a collection chamber. The collection chamber includes a vent having an hydrophobic filter for the passage of air to facilitate the movement of CSF yet to maintain a closed system. The system includes a buoyant float hingedly connected with the top of the collection chamber in one embodiment. When fluid rises in the collection chamber to a predetermined volume, buoyant force raises the float and causes a seal plug mounted on top of the float to seal one of an inflow port or a vent port. The float is limited to pivoting movement in one plane and to a certain angle within that plane. The system and method avoid overdrainage of CSF from the patient and overfilling of the collection chamber. | 2012-11-08 |
| 20120283677 | BODY WASTE COLLECTING DEVICE - The application discloses a body waste collecting device comprising a collecting pouch and an adhesive wafer for attachment to the skin, said wafer comprising a backing layer and a first and second layer of hydrocolloid adhesive, where the second layer of hydrocolloid adhesive is at least partly interposed between the first layer of hydrocolloid adhesive and the backing layer, the first and second adhesive layers consisting of a continuous phase and a discontinuous phase, wherein
| 2012-11-08 |
| 20120283678 | CONTROLLED EVACUATION OSTOMY APPLIANCE - A controlled evacuation ostomy appliance comprises a pouch having a non-entrant stoma seal and a retainer for retaining the lower portion of the pouch in the folded-up condition. The appliance optionally includes a body fitment that may include a region of manually moldable adhesive for forming a custom fit at the stoma. | 2012-11-08 |
| 20120283679 | Belly binder with a reinforced opening - A belly binder for providing support to an ostomy apparatus is disclosed. The belly binder comprises a flexible band, preferably made of a heavy duty elastic material. The band is wrapped around the abdomen of a wearer for support. Fasteners are attached to the ends of the flexible band to hold the band in position. The flexible band comprises, on its surface, an opening that is adapted to receive an ostomy bag. Further, a support member is attached to the flexible band. The support member is such that it forms a pocket/pouch like structure to hold and support the ostomy bag. | 2012-11-08 |
| 20120283680 | Visually-Coordinated Absorbent Product - A visually-coordinated absorbent product includes an absorbent article component including a garment side outer cover and a body side liner, wherein the article component has at least a first and second visual characteristic, and wherein the first visual characteristic is different from the second visual characteristic. The absorbent product also includes a first packaging component including at least first and second visual characteristics, wherein first and second visual characteristics of the absorbent article are coordinated to the first and second visual characteristics of the packaging component, and wherein at least a portion of one of the garment side outer cover and the body side liner is configured with the article component first visual characteristic and at least a portion of one of the garment side outer cover and the body side liner is configured with the article component second visual characteristic. | 2012-11-08 |
| 20120283681 | Web Treatment Apparatus Having Center Bearer Ring And Method Of Using The Apparatus - Apparatus for treating at least one web passing through the apparatus includes a first roller and a second roller positioned adjacent the first roller to define a nip for receiving the at least one web. The first roller has a pair of spaced apart ends, a length extending between the ends, a circumference, and at least one bearer ring extending around the circumference of the first roller generally at a center of the first roller. | 2012-11-08 |
| 20120283682 | DISPOSABLE WEARING ARTICLE - The present invention provides a disposable wearing article having a position indicator mark formed on a crotch member and overlapped by front and rear waist members. Front and rear waist members overlap front and rear ends, respectively, of a crotch member and are bonded thereto to define first and second overlapping regions and an intermediate region extending between these first and second overlapping regions. A position indicator mark is formed in the first overlapping region, a graphic of fish is portrayed as a crotch graphic element in the second overlapping region and graphics of fish are portrayed in the intermediate region as crotch graphic elements. In the first overlapping region, a front waist sheet of the front waist member overlaps a front graphic film on which a graphic of penguin is portrayed as a front graphic element which, in turn, overlaps the position indicator mark. | 2012-11-08 |
| 20120283683 | Diaper - A diaper includes first and second sheets having elastic strings, and a crotch section with an absorbent body connected to the first and second sheets. The first sheet includes two first margins, each of which is contiguous to one of first outermost edges, and a first notch that is indented inwardly from one of the first outermost edges to extend inwardly through and beyond the adjacent first margin. The second sheet includes two second outermost edges, two second margins. The second margins are thermal bonded respectively to the first margins to form thermal seams. The first notch forms a first opening contiguous to one of the thermal seams to provide good ventilation and to ease tearing of the diaper at the thermal seam. | 2012-11-08 |
| 20120283684 | Tampon Absorbent - A tampon absorbent for insertion into a vaginal cavity is provided. The tampon absorbent includes a longitudinal direction and has an insertion end and a withdrawal end. The tampon absorbent includes a first absorbent material portion at the insertion end for capturing body fluid and demonstrating a first expansion capacity, and a second absorbent material portion at the withdrawal end for storing body fluid and demonstrating a second expansion capacity. The second absorbent material portion is partially wrapped around the first absorbent material portion in a direction transverse (perpendicular) to the longitudinal direction, at a bonding region, whereby the first absorbent material portion is bonded to the second absorbent material portion at the bonding region. | 2012-11-08 |
| 20120283685 | Integrated Tampon and Method for Making - A method of integrating a tampon includes providing an absorbent blank having a longitudinal centerline and compressing the absorbent blank in a direction perpendicular to the longitudinal centerline to form a pledget having a compressed diameter. The method also includes penetrating the pledget in the perpendicular direction to a compressed depth of at least 20% of the compressed diameter to form a discrete indentation. | 2012-11-08 |
| 20120283686 | Diaper With Fecal Matter Collector - A disposable diaper for use on babies having an outer barrier layer which is impervious to liquids, an inner barrier layer which comes in contact with a baby's skin, and an intermediate absorptive layer is provided. In one embodiment, the new diaper includes longitudinal skirts for preventing feces from migrating outward of the diaper. In another embodiment, the new diaper is configured into an upper region and a lower region. The upper region captures a baby's urine discharges while the lower region includes a pouch for the capture of feces. The upper and lower regions are separated to prevent the communication of liquid and solid matter between the regions. | 2012-11-08 |
| 20120283687 | DIAPER COVER - A diaper cover comprising a front part, a back part and an intermediate part located between the front part and the back part in a front-back direction, a right waist part and a left waist part extending from the back part in a width direction, and a right flap part and a left flap part extending from the front part in the width direction, wherein each of the right flap part and the left flap part is provided with a first attachment, the right flap part, the left flap part and the intermediate part are stretchable, and the first attachment is attachable to a position on a dorsal side of a wearer in a state where the right flap part and the left flap part are stretched. | 2012-11-08 |
| 20120283688 | HANGER LABEL FOR A LIQUID BAG AND METHOD FOR ATTACHING A LABEL TO A LIQUID-FILLED BAG - A special label is adapted for labeling of infusion bags containing a liquid. The bag is labeled only in a small partial area, which does not contain any liquid. For safe labeling capable of being automated, the label consists of a special film composite, which makes it possible to form a flap with special hinge properties. By virtue of the special fastening options, accidental detachment of the label from the infusion bag is prevented. | 2012-11-08 |
| 20120283689 | Process for preparing a lyophilized material - A process for preparing a lyophilized material, providing a container having a penetrable envelope and containing the material in a carrier liquid, whereby the penetrable region is penetrated with a penetrator which provides a conduit through the envelope, and the carrier liquid is evaporated out of the container via the conduit, after which the penetrator is withdrawn. | 2012-11-08 |
| 20120283690 | ENTERAL FEEDING SAFETY RESERVOIR AND SYSTEM - The present invention provides a one-piece bottle containing enteral feeding material and having a top end with a threaded section and a bottom end comprising a funneled connector port; and a threaded cap dimensioned to mate with the threaded section of the one-piece bottle; wherein the funneled connector port connects to an enteral feeding assembly; wherein the threaded cap provides a leak proof seal when tightened on the threaded section of the one-piece bottle, and allows venting of the bottle when loosened. | 2012-11-08 |
| 20120283691 | AUTOMATED PRESSURE LIMIT SETTING METHOD AND APPARATUS - A method of infusing a fluid includes receiving values of one or more infusion parameters for an infusion of a fluid. Based on the received infusion parameter values, an occlusion pressure threshold for the infusion of the fluid is automatically calculated. During the infusion, a fluid pressure value is sensed. An indication is provided responsive to whether a value of the sensed fluid pressure is greater than the occlusion pressure threshold. | 2012-11-08 |
| 20120283692 | MESH BASED FLUID DELIVERY PROSTHESIS AND METHOD OF USE - A fluid delivery system is used for the treatment of subcutaneous hernia sites and includes a bioabsorbable polymer fabric mesh layer and a bioabsorbable and permeable bladder attached to the upper side of the fabric mesh layer. Fluid from the bladder is diffused through pores communicating between the bladder and the fabric mesh layer so as to be dispersed to underlying tissue. | 2012-11-08 |
| 20120283693 | Antiseptic Cap with Antiseptic - A syringe assembly including: (1) a syringe barrel defining a chamber; (2) a plunger mounted in the chamber and moveable with respect to the barrel; and (3) a cap assembly containing a cap and an absorbent material is removably attached to the plunger. | 2012-11-08 |
| 20120283694 | DEVICES, SYSTEMS AND METHODS FOR QUANTIFYING BOLUS DOSES ACCORDING TO USER PARAMETERS - Devices, systems and methods for determining a recommended bolus dose of therapeutic fluid to be delivered to the body are disclosed. Such a recommended bolus dose may be provided by establishing an initial bolus dose for a user based on one or more first parameters relating to the user and adjusting (e.g., increasing or decreasing) this initial bolus dose amount based on one or more second user parameters by multiplying the initial bolus dose by one or more multiplier values that correlate to at least one of the second parameters and/or by adding or subtracting an absolute value of at least one of the second parameters from the initial bolus dose amount. | 2012-11-08 |
| 20120283695 | TRANSDERMAL DRUG DELIVERY PATCH AND METHOD OF CONTROLLING DRUG RELEASE OF THE SAME BY NEAR-IR - A transdermal drug delivery patch and a method of controlling the drug release of the transdermal drug delivery patch by near-IR are disclosed. The transdermal drug delivery patch comprises a substrate, carriers and drugs. The drugs are encapsulated in the carriers, and the carriers having the drugs are disposed on a surface of the substrate. The carriers are formed of biodegradable polymers, and nano-particles with a photothermal conversion effect are loaded in the carrier. When the carriers are punctured into the skin and the nano-particles in the carrier absorb the near-IR, the near-IR is converted into heat by the nano-particles to melt the carrier and thus releasing the drugs encapsulated in the carrier into the skin. Accordingly, the speed of releasing the drugs encapsulated in the carrier can be controlled accurately by the near-IR. | 2012-11-08 |
| 20120283696 | Self-Injection Device with Multi-Position Cap - A self-injection device ( | 2012-11-08 |
| 20120283697 | METHODS FOR STIMULATING A DORSAL ROOT GANGLION - Some embodiments of the present invention provide stimulation systems and components for selective stimulation and/or neuromodulation of one or more dorsal root ganglia through implantation of an electrode on, in or around a dorsal root ganglia. Some other embodiments of the present invention provide methods for selective neurostimulation of one or more dorsal root ganglia as well as techniques for applying neurostimulation to the spinal cord. Still other embodiments of the present invention provide stimulation systems and components for selective stimulation and/or neuromodulation of one or more dorsal root ganglia through implantation of an electrode on, in or around a dorsal root ganglia in combination with a pharmacological agent. | 2012-11-08 |
| 20120283698 | SYRINGE GUARD WITH SELECTED NEEDLE CONFIGURATIONS - A device for expelling a fluid through a needle mounted on a hub includes an elongated luer member that has a distal portion dimensioned to engage the needle hub to provide fluid communication between the luer member and the needle. An adapter anchors the luer member within the device. Slidingly mounted on the adapter is a cylindrical-shaped inverted plunger that is movable thereon between an advanced position and a withdrawn position. A needle guard is biased by a biasing member to extend distally from the luer member when the plunger is in the advanced position. The guard is selectively engageable with the plunger to be retracted to expose the distal portion of the luer member for fluid engagement with the needle hub when the plunger is moved to the withdrawn position. | 2012-11-08 |
| 20120283699 | APPARATUS AND METHODS FOR CLOT DISSOLUTION - Clot disruption and dissolution are achieved using a catheter having the ability to infuse a thrombolytic agent, aspirate clot and fluid, and allow passage of a guidewire. Optionally, the catheter may also include a mechanical agitator for further disrupt clot in the presence of the thrombolytic agent. A flow resistor in the catheter provides for infusion and/or aspiration to be concentrated primarily at a clot treatment area in a blood vessel while also providing optional infusion and/or aspiration distal to the treatment area. In some embodiments, infusion, aspiration and guidewire passage occur through a common lumen. The thrombolytic agent, such as tPA, streptokinase, or urokinase, is directly released into the clot at the point where the agitator is engaging the clot. In this way, the thrombolytic activity of the agent is enhanced and the dissolution of the clot is improved. | 2012-11-08 |
| 20120283700 | MULTI-METAL GUIDE WIRE COIL - A guide wire includes a distal flexible member, such as a helical coil, which is formed with at least one highly radiopaque component and at least one component that is less radiopaque. A first wire is wound into first coils and a second wire is wound into second coils so that the first coils alternate between the second coils to form a distal helical coil. The second wire is highly radiopaque to assist a physician in positioning the distal end of the guide wire in a patient's vasculature, such as a coronary artery. | 2012-11-08 |
| 20120283701 | CATHETER HAVING AN IMPROVED DISTAL TIP - One embodiment is a medical device comprising an elongate catheter having a proximal end, a distal end, and a lumen extending therethrough and a tip disposed at the distal end of the elongate catheter, the tip extending distally of the distal end of the catheter, the tip comprising a soft body portion and a rigid ring distal the soft body portion. | 2012-11-08 |
| 20120283702 | NEEDLELESS MEDICAL CONNECTOR - A valve for selectively permitting a fluid flow between first and second medical implements is disclosed. The valve has a housing with an interface suitable for receiving a connector portion of a first medical device such as a catheter, and a seal made of a flexible material. The seal has a first end in fluid communication with the interface, a second end suitable for receiving the second medical device, and at least one slit in fluid communication with the first end and the second end. The slit defines a restricted fluid flow path and a relatively small interior volume when in an undisturbed state, defines an expanded fluid flow path and a larger interior volume upon the introduction of the second medical instrument into the slit, and retracts to define a restricted flow path and a small interior volume upon the withdrawal of the second medical device from the seal. | 2012-11-08 |
| 20120283703 | Flow Rate Accuracy of a Fluidic Delivery System - Improving the accuracy of the flow rate of a valve in a fluidic delivery device in which a desired flow rate may be achieved by varying the duty cycle of the valve. The flow rate of fluid delivery from the valve over its lifetime is stabilized by minimizing the voltage OPENING time of the valve to account for valve and piezoelectric actuator drift. Also, the valve OPENING time of one or more fluidic parameters that impact on the flow rate delivery by the valve and differ among fluidic delivery devices is compensated to optimize the flow rate accuracy. | 2012-11-08 |
| 20120283704 | DRUG INFUSION SYSTEM AND METHOD ADAPTED TO START DURING PROGRAMMING CYCLE - Drug infusion system capable of delivering a fluid medication to a patient and method for doing same is described. An implantable drug delivery device is capable of delivering the fluid medication at a programmable rate to the patient under control of an original programming cycle having a plurality of steps in a plurality of time slots beginning at a starting time. The programming cycle specifies the programmable rate for each of the plurality of steps. An external controller is capable of storing a program representative of the original programming cycle in the implantable drug delivery device at a programming time. The drug infusion system adjusts the implantable drug delivery device so that the original programming cycle will begin at a time during the original programming cycle adjusted for the programming time. | 2012-11-08 |
| 20120283705 | PERCUTANEOUS DELIVERY TOOL - A percutaneous delivery tool may be used to implant a medical device, for example, within a subcutaneous space. The percutaneous delivery tool may include a handle, first and second attachment members, and first and second connecting members connecting the attachment members to the handle. In some examples, the first and second attachment members are configured to receive the medical device such that the medical device is positioned between the attachment members. In some additional examples, the first and second connecting members are angled with respect to the handle, the first connecting member is angled with respect to the first attachment member, and the second connecting member is angled with respect to the second attachment member. | 2012-11-08 |
| 20120283706 | SURGICAL INSTRUMENT, SURGICAL HANDPIECE AND SURGICAL DRIVE SYSTEM - In order to improve a surgical instrument comprising a shank and a drive shaft, which is rotatably mounted in the shank and bears or comprises a tool element at its distal end, wherein in the distal end region of the shank a radial bearing is arranged or configured for the rotatable mounting of the drive shaft on the shank, such that a reliable operation is possible even with increasing miniaturisation of the shanks, it is proposed that the radial bearing is configured in the form of a needle bearing. | 2012-11-08 |
| 20120283707 | SURGICAL INSTRUMENT WITH WIRELESS COMMUNICATION BETWEEN CONTROL UNIT AND REMOTE SENSOR - A surgical instrument including an end effector having at least one sensor. The instrument includes a distal stapling unit for performing at least one surgical task operatively connected to a remotely controllable user interface. The instrument further includes an electrically conductive shaft having a distal end connected to the end effector, wherein the sensor is electrically insulated from the shaft. The instrument also includes a housing at a proximate end of the shaft configured to receive mechanical or electrical inputs. In addition, the instrument has a receiver unit electrically insulated from the shaft configured to receive and send wireless signals from and to the sensor. | 2012-11-08 |
| 20120283708 | ADJUSTING OPHTHALMIC DOCKING SYSTEM - An adjusting ophthalmic docking system is described that includes a curved contact element, disposed on a procedure eye, a conformation platform at a distal tip of an optical system to support an adjustment of the curved contact element, and a connector to accommodate the adjustment of the contact element. The curved contact element can be a meniscus-shaped contact lens, with a proximal surface radius larger than a distal surface radius. The contact lens can be made of an approximately refractive index-matching material, such as a fluoro-polymer. | 2012-11-08 |
| 20120283709 | Devices and Methods for Radiation-Based Dermatological Treatments - A self-contained, hand-held device for providing a dermatological treatment includes a radiation source configured to generate one or more radiation beams, and an optical system configured to deliver the one or more radiation beams to the skin to provide a dermatological treatment. Each radiation beam includes a first axis beam profile and an orthogonal second axis beam profile. The optical system includes a first axis optic configured to influence the first axis beam profile of each radiation beam by a greater extent than the second axis beam profile of each radiation beam, and a second axis optic configured to influence the second axis beam profile of each radiation beam by a greater extent than the first axis beam profile of each radiation beam. | 2012-11-08 |
| 20120283710 | Devices and Methods for Radiation-Based Dermatological Treatments - A hand-held device for providing laser-based dermatological treatments includes a laser beam source supported in a device body, an automated scanning system, and control electronics. The automated scanning system is configured to receive an input beam generated by the laser beam source and scan the input beam to provide a series of output beams for delivery to the skin via an application end of the device to form a pattern of treatment spots on the skin. The application end is configured for movement across the skin during a treatment session. The control electronics control the laser beam source and/or the automated scanning system to deliver the scanned output beams to the skin at a radiation intensity sufficient to provide an effective dermatological treatment, and wherein the scanned output beams delivered from the application end of the device meet the Class 1M or better eye safety classification per the IEC 60825-1. | 2012-11-08 |
| 20120283711 | Devices and Methods for Radiation-Based Dermatological Treatments - A device for providing a dermatological treatment, the device includes a device body, a radiation delivery system for delivering radiation to the skin to provide a dermatological treatment, and a situation-specific control system. The control system includes a plurality of sensors and control electronics programmed to receive signals from the plurality of sensors; determine whether to initiate radiation delivery by the radiation delivery system based on a comparison of the signals received from the plurality of sensors to a first condition; and once radiation is initiated, determine whether to continue radiation delivery by the radiation delivery system based on a comparison of the signals received from the plurality of sensors to a second condition that is different than the first condition. | 2012-11-08 |
| 20120283712 | Devices and Methods for Radiation-Based Dermatological Treatments - A hand-held device for providing a dermatological treatment by scanning a laser beam to form a pattern of treatment spots on the skin includes a laser source that generates an input beam, an automated scanning system, and a treatment spot control system. The automated scanning system includes a rotating multi-sector scanning element configured to repeatedly scan the input beam, each scan providing an array of output beams corresponding to the multiple sectors of the scanning element and forming a scanned row of treatment spots on the skin. The scanning element is configured such that each sector provides a constant-angular-direction output beam as that sector rotates through the input beam. The treatment spots of each scanned row are spaced apart from each other by areas of non-irradiated skin. The treatment spot control system provides a distance between adjacent rows of treatment spots in a direction of manual movement of the device. | 2012-11-08 |
| 20120283713 | COMPLIANT SLEEVES COUPLED WITH WIRE STRUCTURES FOR CRYOABLATION - A medical system, including a catheter body, a mesh coupled to the catheter body; an expandable element enclosing the mesh, the expandable element made from a compliant natural rubber emulsion, such as Yulex® HA; and a cryogenic coolant source in fluid communication with the expandable element. | 2012-11-08 |
| 20120283714 | METHODS OF TREATMENT WITH COMPLIANT ELEMENTS AND WIRE STRUCTURES - A method of treating a tissue region, including deploying a plurality of sensors of a medical device into contact with the tissue region; measuring at least one of an electrical voltage, capacitance or resistance value with at least one of the plurality of sensors; generating a position indicator based at least in part on the measured value; inflating an expandable element of the medical device, and thermally affecting the tissue region with the expandable element. | 2012-11-08 |
| 20120283715 | ELECTRICAL SENSING SYSTEMS AND METHODS OF USE FOR TREATING TISSUE - A medical system, including a catheter body, an expandable element coupled to the catheter body; a first electrically-conductive element coupled to an interior surface of the expandable element; and a second electrically-conductive element coupled to an exterior surface of the expandable element, where the first and second electrically-conductive elements form a capacitor with the expandable element. | 2012-11-08 |
| 20120283716 | ABLATION DEVICES AND METHODS OF USE - Described herein are various methods and devices for delivering cryoablative therapy. One such device includes a cryoablation chamber and a volume displacement chamber. In use, the volume displacement chamber can be expanded to occupy a non-therapeutic volume. | 2012-11-08 |
| 20120283717 | Uterine Therapy Device and Method - A method and system of providing therapy to a patient's uterus. The system has an access tool with a lumen, the access tool being adapted to be inserted through a human cervical canal to place an opening of the lumen within a uterus when the access tool is inserted through the cervical canal; a seal disposed at a distal region of the access tool and adapted to seal the access tool against an interior cervical os; a sealing indicator adapted to provide a user with an indication that the seal has sealed the access tool with the interior cervical os; and a vapor delivery mechanism adapted to deliver condensable vapor through the access tool to the uterus, the condensable vapor being adapted to condense within the uterus. | 2012-11-08 |
| 20120283718 | LIGHT ATTACHMENT DEVICE FOR ELECTROSURGICAL PENCIL AND ELECTROSURGICAL PENCIL ATTACHMENTS - A light attachment device for removable attachment to an electrosurgical pencil and/or an electrosurgical pencil attachment such as a shroud for an electrosurgical pencil. The light attachment device may be automatically turned on and off in conjunction with the activation and deactivation of the electrosurgical pencil and/or electrosurgical pencil attachment. | 2012-11-08 |
| 20120283719 | CATHETER WITH TISSUE PROTECTING ASSEMBLY - A medical probe includes an elongate member having a proximal end and a distal end, an ablative element mounted to the distal end of the elongate member, and a cage assembly mounted to the distal end of the elongate member, the cage assembly at least partially covers the ablative element. A method of treating tissue in a body includes inserting an ablative element in the body, placing the ablative element adjacent the tissue, and maintaining a distance between the ablative element and the tissue using a protective catheter element that circumscribes at least a portion of the ablative element. | 2012-11-08 |
| 20120283720 | Combined Bipolar and Monopolar Electrosurgical Instrument and Method - An electrical switching system for use in various types of electrosurgical instruments and related tools comprises a system adapted to automatically determine which of at least two electrical current modes to deliver through an electrosurgical instrument based on a condition sensed by the electrosurgical instrument. In another embodiment, the electrical switching system comprises a generator, the generator including a first electrical distribution systems for delivering monopolar electrical energy, and a second electrical distribution system for delivering bipolar electrical energy, a controller coupled to the generator for selecting based on an input which of the first and second electrical distribution systems to activate. | 2012-11-08 |
| 20120283721 | Temperature Monitoring Return Electrode - An electrosurgical return electrode is disclosed. The return electrode includes a first and second flexible conductive material layers and a material layer disposed between the first and second conductive material layers. The material layer is transitionable between a solid state and a non-solid state, the material layer is also configured to melt upon an increase in temperature beyond a predetermined threshold, thereby increasing conductivity between the first and second conductive material layer. | 2012-11-08 |
| 20120283722 | ADIABATIC COOLING SYSTEM FOR MEDICAL DEVICES - A medical treatment system, including a catheter body defining a proximal end and a distal end; an ablation element coupled to the catheter body and defining a fluid flow path therethrough, the ablation element including a first segment disposed within the catheter body, a second segment extending out of the distal end of the catheter body, and a third segment coiled around the first segment; and a coolant supply in fluid communication with the fluid flow path. | 2012-11-08 |
| 20120283723 | ELECTROSURGICAL INSTRUMENT - A bipolar snare including an elongated tubular electrically insulating sheath, a pair of elongated flexible electrically conductive wires disposed within the sheath, and an electrically insulating connector disposed at the distal ends of the wires mechanically connecting the distal ends of the wires to form a loop projecting from the distal end of the sheath. The wires are provided with electrical insulation covering all but a selected portion of each of the wires. The device also includes a guide member located within the sheath and forming compartments for each of the electrically conductive wires, the guide member being rotatable within the sheath. The guide member is also set back from the distal end of the sheath to an extent such that the whole of the loop including at least part of the connector is capable of being received within the sheath. | 2012-11-08 |
| 20120283724 | METHODS FOR EVALUATING THE INTEGRITY OF A UTERINE CAVITY - Methods, systems and devices for evaluating the integrity of a uterine cavity. A method comprises introducing transcervically a probe into a patient's uterine cavity, providing a flow of a fluid (e.g., CO | 2012-11-08 |
| 20120283725 | METHODS FOR CREATING TISSUE EFFECT UTILIZING ELECTROMAGNETIC ENERGY AND A REVERSE THERMAL GRADIENT - A method of creating a tissue effect at a tissue site delivers electromagnetic energy through a skin surface from an electromagnetic energy delivery device coupled to an electromagnetic energy source. At least one of the electromagnetic energy delivery device or electromagnetic energy source includes a memory. A reverse thermal gradient is created through the skin surface to sufficiently heat an underlying tissue site to provide that a temperature of the skin surface is lower than a temperature of the underlying tissue. Information is stored from the memory to facilitate operation of at least one of the electromagnetic energy delivery device or the electromagnetic energy source. Electromagnetic energy is applied through the skin surface to the underlying tissue. A tissue effect is created on at least a portion of the tissue site. | 2012-11-08 |
| 20120283726 | TREATING A TUMOR OR THE LIKE WITH ELECTRIC FIELDS AT DIFFERENT FREQUENCIES - Cells that are in the late anaphase or telophase stages of cell division are vulnerable to damage by AC electric fields that have specific frequency and field strength characteristics. The selective destruction of rapidly dividing cells can therefore be accomplished by imposing an AC electric field in a target region for extended periods of time. Some of the cells that divide while the field is applied will be damaged, but the cells that do not divide will not be harmed. This selectively damages rapidly dividing cells like tumor cells, but does not harm normal cells that are not dividing. Improved results may be achieved by using a field with two or more frequencies. | 2012-11-08 |
| 20120283727 | Surgical Forceps - A forceps includes an end effector assembly having first and second jaw members disposed in opposed relation relative to one another. One (or both) of the jaw members is moveable with respect to the other from a spaced-apart position to an approximated position for grasping tissue therebetween. A knife is longitudinally translatable with respect to the first and second jaw members between a retracted position, an intermediate position, and an extended position. The knife coupled to one or both of the jaw members via a pin-slot engagement such that, upon translation of the knife from the retracted position to the intermediate position, the first and second jaw members are moved to the approximated position to grasp tissue therebetween and such that, upon translation of the knife from the intermediate position to the extended position, the knife is extended between the jaw members to cut tissue grasped therebetween. | 2012-11-08 |
| 20120283728 | ELECTROSURGICAL UNIT PENCIL APPARATUS AND SHROUD HAVING DIRECTED ILLUMINATION - An electrosurgery pencil having directed illumination and a removable shroud having directed illumination where the removable shroud is adapted to fit over an electrosurgery pencil. | 2012-11-08 |
| 20120283729 | Vessel Sealer and Divider with Knife Lockout - An endoscopic forceps includes a housing having a shaft attached thereto that supports a pair of jaws disposed at a distal end thereof. A drive assembly having a drive shaft with a proximal end is operable to move the jaws relative to one another from an open to closed positions. A knife assembly is operable to advance a knife through tissue disposed between the jaws and includes a flange disposed thereon. A knife lockout is included that has a flange configured to engage the proximal end of the drive shaft and a lockout arm configured to engage the flange of the knife assembly to prevent movement thereof. Movement of the jaws to the closed position causes the proximal end of the drive shaft to engage the flange on the lockout which causes the lockout arm to disengage the flange on the knife assembly to permit advancement of the knife. | 2012-11-08 |
| 20120283730 | METHOD AND DEVICE FOR TISSUE FUSION OR COAGULATION BY TISSUE RESISTANCE-DEPENDENT VOLTAGE-CONTROLLED ELECTRICAL ACTION - In the method suitable for tissue fusion or coagulation after the commencement of treatment of the tissue, i.e., after completion of a first phase, a second phase is commenced, during which the biological tissue is treated with moderate energy for a certain specified process time. The specification of a functional relationship between the tissue resistance and the output voltage of a supplying source enables the process in phase II to not fall below a minimum treatment time, avoiding premature drying-out of the tissue. A sufficient and reliable bonding of the participating proteins in a moist milieu is reached. | 2012-11-08 |
| 20120283731 | System and Method for Tissue Sealing - An electrosurgical generator is disclosed. The generator includes an RF output stage configured to supply electrosurgical energy to tissue via at least one active electrode configured to apply electrosurgical energy to tissue; sensing circuitry configured to measure impedance of tissue; and a controller. The controller is configured to determine occurrence of a tissue reaction as a function of a minimum impedance value and a predetermined rise in impedance, wherein tissue reaction corresponds to a boiling point of tissue fluid; generate a target impedance trajectory as a function of measured impedance and desired rate of change based on the tissue reaction determination, wherein the target impedance trajectory includes a plurality of target impedance values; and drive tissue impedance along the target impedance trajectory by adjusting the output of the electrosurgical generator to substantially match tissue impedance to a corresponding target impedance for at least a predetermined minimum time period. | 2012-11-08 |
| 20120283732 | PLASMA HEAD FOR TISSUE WELDING - A compact medical device for tissue welding is provided. The hand-held plasma heads are configured for deep cuts and long cuts. A bio-compatible liquid capable of solidifying in response to application of plasma, such as an albumin solution, is applied to the wound. Plasma created from a gas such as helium is then applied to said bio-compatible liquid to solidify it and seal the wound. An additional polymerizing gas may also be applied. A feedback mechanism may maintain the temperature of said plasma. A wiper fort removal of excess liquid may also be provided. | 2012-11-08 |
| 20120283733 | METHOD AND DEVICE FOR TISSUE FUSION OR COAGULATION BY AN ELECTRICAL ACTION WITH NEGATIVE SOURCE IMPEDANCE - In a method suitable for tissue fusion or coagulation, after the start of treatment of the tissue, i.e., after completion of a first phase, a second phase is commenced, during which the biological tissue is treated for a certain specified process time with moderate energy input. The specification of a negative internal resistance of a supplying source enables the process in the second phase to have a treatment time that remains constant and thus avoids premature drying-out of the tissue. A sufficient and reliable bonding of the participating proteins in the moist milieu is reached. | 2012-11-08 |
| 20120283734 | Bifurcated Shaft for Surgical Instrument - A surgical instrument includes a shaft having a proximal end and a bifurcated distal end defining a first shaft portion and a second shaft portion. An end effector assembly is disposed at the distal end of the shaft and includes first and second jaw members. One (or both) of the jaw members is moveable relative to the other between an open position and a closed position for grasping tissue therebetween. Each of the jaw members defines an opposed jaw surface and is independently coupled to one of the first and second shaft portions. The first and second shaft portions are configured to flex relative to one another during movement of the jaw members to the closed position to grasp tissue therebetween such that the opposed jaw surfaces of the jaw members are disposed in substantially parallel orientation relative to one another when grasping tissue therebetween. | 2012-11-08 |
| 20120283735 | RADIO-FREQUENCY TISSUE WELDER TWO STAGE PRESSURE APPLICATION - There are disclosed methods and apparatus for attachment and welding of tissue. In an embodiment, the apparatus includes an energy applicator configured to apply energy to generate heat within a target tissue to evaporate water to create dried tissue, and a thermally conductive material disposed adjacent the first tissue contacting surface or the second tissue contacting surface. The thermally conductive material may be configured for direct contact with the target tissue heated by the energy applicator. The thermally conductive material provides a high coefficient of thermal conductivity so as to evenly distribute heat within the targeted tissue area. Other embodiments are also disclosed. | 2012-11-08 |
| 20120283736 | EXTERNAL FIXATOR - A fixator for use in the reconstruction of acute, chronic and traumatic injuries to the upper and lower extremities. The fixator has a unique clamping system that allows for the snapping in of pins and rails, and for multi-planar fixation of bones. | 2012-11-08 |
| 20120283737 | Guide Tube Positioning Method in Polymeric Material Plate, Tomographic Reference Support and Guide Tube Positioning Device - A method is described for positioning a guide tube on a plate to be positioned over a patient's mandible or maxilla, forming a surgical guide that allows for positioning the guide tube on the exact position so as to enable the drilling of a perfect hole in the patient's bone portion and the subsequent positioning of an implant exactly on the planned spot. A tomographic reference support is described for fixing a guide tube positioning device, and a guide tube positioning device is described for positioning one or more guide tubes on an acrylic plate or the like, configuring a surgical guide. | 2012-11-08 |
| 20120283738 | MIDLINE REFERENCING FEMORAL SIZING CALIPER - A sizing caliper for facilitating the selection of a femoral component of a knee prosthesis includes a caliper body, a drill guide body, a stylus tower and a graduated stylus slidably coupled to the stylus tower. The caliper body, the stylus tower and the two drill guide body portions are configured to be slidably linked to each other, whereby as the caliper body and the stylus tower are linearly displaced, in opposite directions along the longitudinal axis L of the sizing caliper, relative to the two drill guide body portions, the caliper body and the stylus tower are linearly displaced at an equal rate relative to the drill guide body portions and the drill guide holes remain located at the midpoint of an anterior/posterior dimension defined by the distance between the tip of the stylus and the base portion. | 2012-11-08 |
| 20120283739 | BONE TACK DRIVER - A driver assembly for affixing a surgical fastener to a target location is provided. Operation of the driver assembly inserts the surgical fastener in two stages, first an alignment stage through application of a distally directed force to partially insert the surgical fastener, and then a fastening stage to fully insert and seat the surgical fastener to a proper depth or compression level. The driver assembly comprises a spring loaded automatic trigger mechanism that may be adapted for use with a linearly insertable or a rotationally insertable surgical fastener. Application of the distally directed force actuates the trigger mechanism, wherein a corresponding impact force is delivered for seating the surgical fastener, coupled to a distal end of the driver assembly, upon alignment of cam and receiver elements embodied within the trigger mechanism. | 2012-11-08 |
| 20120283740 | SURGICAL HANDPIECE - The present invention relates to a surgical handpiece for driving a surgical tool, with a housing, in which there are arranged a drive in the form of a compressed air motor and at least one bearing or gear part cooperating with the drive on the output side, further comprising at least one lubricant spray connection for coupling to a lubricant spray source, and which is in fluidic connection with at least one of the at least one bearing or gear part and the compressed air motor. | 2012-11-08 |
| 20120283741 | RETRACTABLE TIP FOR VITRECTOMY TOOL - A probe for a vitrectomy tool is provided having a vitreous cutter tube having a blunt tip at a distal end and adapted to be coupled at a proximal end to a handpiece of a vitrectomy tool; a retractable outer trocar tube surrounding the vitreous cutter tube having an open distal end with a sharpened edge; and a retraction mechanism coupled to a proximal end of the outer trocar for selectively extending and retracting the outer trocar tube between a first extended position wherein the sharpened edge of the outer trocar is extended beyond the blunt tip of the vitreous cutter tube to facilitate insertion into the eye and a second retracted position wherein the sharpened edge of the outer trocar is retracted behind the blunt tip of the vitreous cutter tube to facilitate safe operation of the probe. | 2012-11-08 |
| 20120283742 | DEVICES AND METHODS FOR CUTTING TISSUE - Various medical devices and methods for cutting and/or evacuating tissue are provided. The devices and methods may utilize a reciprocating mechanism or motor powered by suction from a vacuum source. The medical devices and methods may be used on tissue in various regions of a patient's body and for treating various conditions, e.g., for performing a polypectomy or discectomy. | 2012-11-08 |
| 20120283743 | ULTRASOUND CATHETER HAVING IMPROVED DISTAL END - An ultrasound catheter has an elongate flexible catheter body having a lumen extending longitudinally therethrough, and an ultrasound transmission member extending longitudinally through the lumen of the catheter body. The ultrasound transmission member has a proximal end that is coupled to a separate ultrasound generating device, and a distal tip that is attached to the distal end of the ultrasound transmission member and which is located at the distal end of the catheter body. The distal tip has at least one dimensional step. The ultrasound transmission member is directly attached to the catheter body and/or to a guidewire tube, either directly or via an attachment device. The catheter has an additional radiopaque marker positioned on the distal end the catheter. | 2012-11-08 |
| 20120283744 | INSERTION TOOL FOR A SPINAL CORD STIMULATION ELECTRODE - The present invention is directed to an insertion tool for a spinal cord stimulation electrode. The insertion tool comprises a first leg and a second leg coupled to the first leg. The first and second legs are separable for placement around the electrode and resiliently return to a clamped position. Each of the first and second legs generally defines a respective longitudinal axis. Each of the first and second legs defines a blade portion offset from the respective longitudinal axis for clamping the electrode. | 2012-11-08 |
| 20120283745 | SELECTIVE ADDITIONAL CONTROL IN A CONTROL CONSOLE FOR SURGICAL INSTRUMENTS - A control console to remotely control medical equipment is disclosed having a base with an ergonomically adjustable pedal system. The base further has an opening to receive the pedal system. The pedal system includes a moveable pedal tray with a pedal base. The tray includes a first left pedal assembly and a first right pedal assembly, and an upper tier having a second left pedal assembly and a second right pedal assembly respectively in alignment with and elevated above the first left pedal assembly and the first right pedal assembly. Rollers are rotatable coupled to the moveable pedal tray to allow it roll over a floor. A drive assembly is coupled between the moveable pedal tray and the base. The drive assembly applies a force to the to roll the moveable pedal tray over the floor within the opening of the base. | 2012-11-08 |
| 20120283746 | Mobile Medical Robotic System - A medical robotic system comprises a drive track unit being operable for moving the medical robotic system along a floor. An upper torso unit is joined to the drive track unit. The upper torso unit comprises at least one actuator assembly. At least one bimanual dexterous manipulator is joined to the actuator assembly in which the actuator assembly imparts torque and movement to the bimanual dexterous manipulator for lifting an object. The bimanual dexterous manipulator comprises a pair of dexterous manipulators. Each of the dexterous manipulators comprises a length being configured to support lifting an adult patient, and an end comprising a planar structure being configured for placing between the adult patient and a patient platform. The drive track unit is operable for moving the medical robotic system to the patient platform and the bimanual dexterous manipulator is operable for lifting the adult patient from the patient platform. | 2012-11-08 |
| 20120283747 | HUMAN-ROBOT SHARED CONTROL FOR ENDOSCOPIC ASSISTANT ROBOT - A surgical system includes a robot with both an active mode and an inactive mode of operation, and a holding arm for holding a surgical tool, and an immediate deactivator for determining when a human operator manually manipulates a holding arm or a surgical tool depending on signals from at least one condition sensor. Immediately upon that determination, the immediate deactivator deactivates the robot. The holding arm includes a stiffener/destiffener for increasing or decreasing the flexibility of the holding arm. The stiffness of the holding arm can be sufficiently decreased in the inactive mode to allow a human operator to skillfully control repositioning the surgical tool into a new position while the flexible holding arm is connected between the robot and the surgical tool. Also, the stiffness of the holding arm can be sufficiently increased, for essentially locking it into a rigid fixed shape for providing sufficient rigidity in the active mode for the robot to reposition the rigid holding arm for repositioning the surgical tool to perform preprogrammed tasks initiated by surgeon command inputs. The holding arm is completely inactive in both the active and inactive modes of the robot. | 2012-11-08 |
| 20120283748 | SURGICAL FASTENER AND CUTTER WITH MIMICKING END EFFECTOR - Methods and devices are provided for controlling movement of a working end of a surgical device. In one embodiment, methods and devices are provided for moving an end effector on a distal end of a surgical fastening device. Movement can include rotational movement of the end effector about an axis of the shaft, articulation of the end effector relative to the shaft, and actuation of an end effector, e.g., closing, firing, and/or cutting. In other embodiments, a single cable actuator is provided and is movable between a first position, in which it is effective to rotate an end effector without actuating (i.e., closing and firing) the end effector, and a second position, in which it is effective to actuate the end effector without rotating the end effector. In other aspects, methods and devices are provided for moving a flexible neck formed on a distal end of an accessory channel for use with an endoscope. Movement of the flexible neck can be used to control positioning of a tool extending through the flexible neck. | 2012-11-08 |
| 20120283749 | MULTIPLE LOOP DEVICE FOR PASSING SUTURE TAILS THROUGH A SURGICAL PLEDGET - A surgical pledget assembly includes a pledget body having first and second apertures extending through the body, one or more snares passing through the apertures in the pledget body and including first and second suture engaging loops disposed on a distal side of the pledget, an optional third folding loop disposed on a proximal side of the pledget, and a handle secured to the ends of the snare or snares proximal to the pledget. | 2012-11-08 |
| 20120283750 | MENISCUS REPAIR - Methods for repairing a meniscus, and particularly a torn meniscus. A method of repairing a meniscus may include using a suture passer to pass a suturing element from the region between the superior surface of the meniscus and the femoral condyle, through the meniscus tissue, into the region between the inferior surface of the meniscus and the tibial plateau, across the inferior surface of the meniscus, and back to the superior surface of the meniscus, without deeply penetrating the posterior capsular region of the knee. Equivalently, the suture element may be passed from the inferior surface of the meniscus to the superior surface and back to the inferior surface. | 2012-11-08 |
| 20120283751 | NEEDLE AND SUTURE DELIVERY DEVICE - A needle delivery device that has particular application for providing needles for minimally invasive spinal surgical procedures. The device includes an elongated pincher having opposing rails that is slidable within a channel defined in an extended base portion. Widened end portions of the rails hold the needle and push it out of an end of the device where it is released. The pincher is then retracted to a location where the end portions can pick up a next needle to be delivered. | 2012-11-08 |
| 20120283752 | Suturing Devices and Methods for Closing a Patent Foramen Ovale - Methods and apparatuses are disclosed for closing a patent foramen ovale. Some of the disclosed apparatuses include an elongate body having a proximal end and a distal end, with first and second suture clasp arms adapted to hold end portions of a suture when in an extended position. A first suture catch mechanism is slidably housed in the elongate body and moves in a proximal-to-distal direction to engage the suture end held by the first suture clasp arm, and a second suture catch mechanism is slidably housed in the elongate body and moves in a distal-to-proximal direction to suture end held by the second suture clasp arm. The first suture clasp arm can be positioned around the septum primum to deliver a suture thereto, and the second suture clasp arm can be positioned around the septum secundum to deliver a suture thereto. | 2012-11-08 |
| 20120283753 | SUTURE PASSER DEVICES AND METHODS - Devices, systems and methods for passing a suture. In general, described herein are suturing devices, such as suture passers, as well as methods of suturing tissue. These suture passing devices are dual deployment suture passers in which a first distal jaw member is moveable at an angle with respect to the longitudinal axis of the elongate body of the device and the second distal jaw member is retractable proximally to the distal end region of the elongate body and/or the first jaw member. Methods of suturing tissue using a dual deployment suture passer are also described. | 2012-11-08 |
| 20120283754 | SUTURE PASSER DEVICES AND METHODS - Devices, systems and methods for passing a suture. In general, described herein are suturing devices, such as suture passers, as well as methods of suturing tissue. These suture passing devices may include dual deployment suture passers in which a first distal jaw member is movable at an angle with respect to the longitudinal axis of the elongate body of the device and the second distal jaw member is retractable proximally to the distal end region of the elongate body and/or the first jaw member. Also described herein are suture passers in which the tissue penetrator passing the suture travels in an approximately sigmoidal pathway, with the distal end of the tissue penetrator extending distally from one jaw of the device. | 2012-11-08 |
| 20120283755 | SUTURING INSTRUMENT - Suturing instruments in accordance with the invention are dimensioned and configured to apply sutures to approximate, ligate, or fixate tissue in, for example, open, mini-incision, transvaginal, laparoscopic, or endoscopic surgical procedures. In some embodiments, the suturing instruments include a distal portion that is deflectably and/or pivotally coupled to the remainder of the instrument for improved maneuverability and functionality during surgery. In other embodiments, the suturing instruments are capable of housing multiple needle and suture assemblies and/or reloading the needle and suture assembly without removing the instrument from the surgical site. | 2012-11-08 |
| 20120283756 | TREATMENT OF HYPERTENSION AND HEART DISEASE VIA SURGERY OF THE STOMACH - Devices and methods for endolumenally manipulating stomach fundus tissue alter the function of nearby nerves. The altered function of the nerves interacts with the cardiopulmonary system to cause a substantially permanent reduction in blood pressure. The altered nerve function may also treat heart disease as well. This application also relates to devices and methods for endolumenally manipulating stomach tissue to alter hormone production from cells associated with stomach tissue, providing a therapeutic effect in treating hypertension and heart disease, not conventionally associated with the stomach. | 2012-11-08 |
| 20120283757 | TISSUE ANCHOR FOR ANNULOPLASTY DEVICE - Apparatus for use with an implant configured to be coupled to cardiac tissue of a patient, the apparatus including: a tissue anchor including: a distal tissue coupling element configured to couple the tissue anchor to the cardiac tissue of the patient, and a proximal implant-receiving element configured to receive at least a portion of the implant and facilitate coupling of the implant to the tissue anchor. The proximal implant-receiving element includes an implant-restraining element coupled to a portion of the implant-receiving element, the implant-restraining element being configured to restrain the implant from separating from the implant-receiving element. Other applications are also described. | 2012-11-08 |
| 20120283758 | METHOD AND APPARATUS FOR TREATING VARICOSE VEINS - Apparatus for occluding a blood vessel, the apparatus comprising: | 2012-11-08 |
| 20120283759 | METHODS AND APPARATUS FOR CROSSING OCCLUSIONS IN BLOOD VESSELS - This disclosure is directed to a device for facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The device includes an intravascular device including a shaft having a distal end and a proximal end. The device includes a handle assembly fixed about the proximal end of the shaft, the handle assembly including a first portion. Rotation of the first portion in a first direction about a longitudinal axis of the shaft causes rotation of the shaft in the first direction when a torque applied by the first portion to the shaft is below a first maximum torque. Further rotation of the first portion in the first direction about a longitudinal axis of the shaft does not cause rotation of the shaft in the first direction when the torque applied by the first portion to the shaft is equal to or above the first maximum torque. | 2012-11-08 |
| 20120283760 | SYSTEMS, METHODS AND DEVICES FOR REMOVING OBSTRUCTIONS FROM A BLOOD VESSEL - Devices and methods for removing an obstruction from a blood vessel are described. The devices are deployed in a collapsed condition and are then expanded within the body. The devices are then manipulated to engage and remove the obstruction. | 2012-11-08 |
| 20120283761 | METHODS AND DEVICES FOR CUTTING TISSUE AT A VASCULAR LOCATION - A tissue cutting device includes a sizing element which detects the diameter of the vessel in which the cutting device is positioned. The sizing element is coupled to the cutting element so that the amount of the cutting element that is exposed varies in response to movement of the sizing element. | 2012-11-08 |
| 20120283762 | Methods of Using Multilayer Medical Sponges - A method of protecting sensitive tissue from damage during a surgical procedure using at least one medical tool having a rotatable bit capable of removing tissue, including selecting a multilayer sponge having (i) a tissue-compatible layer with a tissue contact surface capable of being placed against the sensitive tissue, and (ii) a low-friction layer having a lower coefficient of friction than that of the tissue-compatible layer, being affixed to the tissue-compatible layer, and having an outward-facing surface including biocompatible material not easily worn away by brief contact with the rotatable bit during the surgical procedure. The method further includes placing the tissue contact surface of the biocompatible layer against sensitive tissue such that the outward-facing surface of the low-friction layer is positioned between the sensitive tissue and the rotatable bit to protect the sensitive tissue from damage and prevent the sponge from being drawn around the bit when it rotates. | 2012-11-08 |
