Abstract: An implantable medical device (IMD) has a housing enclosing an electronic circuit. The housing includes a first housing portion, a second housing portion and a joint coupling the first housing portion to the second housing portion. A polymer seal is positioned in the joint in various embodiments. Other embodiments of an IMD housing are disclosed.

Abstract: A device and method for delivering a vascular device to a target site is provided that allows an orientation of the vascular device at the target site to be adjusted by a user. In general, the delivery device includes an outer tubular member, an intermediate tubular member within the outer tubular member, and an inner member that can move axially within the intermediate tubular member. Each of the members defines a proximal end and a distal end. The intermediate and outer tubular members are fixed at their respective proximal ends, but are not fixed at their distal ends. Thus, a torque applied to the proximal end of the intermediate tubular member is at least partially transmitted to the distal end of the intermediate tubular member, allowing the user to rotate an attached vascular device by rotating the proximal end of the intermediate tubular member.

Abstract: A medical device is provided in which one or both ends of the device encourage the formation of tissue across substantially the entire area of the respective end that is exposed to the blood flow for reducing the risk of a thrombotic embolism. The medical device includes a tubular structure having at least one expanded volume portion and a tapered transition portion. The tubular structure may be made through the braiding of a number of strands, and a first end feature may be used to secure the proximal strand ends. The proximal strand ends may be secured via the proximal end of the first end feature, such that the tapered transition portion is formed over the circumferential surface of the first end feature, and only a proximal end surface (or a portion of the proximal end surface) of the first end feature is exposed to the path of flowing blood.

Abstract: The invention relates to a device comprising a surgical material and a support material and related methods for the application of the surgical material to a wound or surgical site using the device.

Abstract: A device for treating tissue includes a capsule extending longitudinally from a proximal end to a distal end and including a lumen extending therein and a clip slidably received within the lumen of the capsule. The clip includes a middle prong, a first outer prong and a second outer prong. The first prong is coupled to the middle prong so that the first prong is movable relative to the middle prong between a first open configuration and a first closed configuration. The second outer prong coupled to the middle prong so that the second prong is movable relative to the middle prong between a second open configuration and a second closed configuration. The first and second outer prongs are independently movable relative to the middle prong to be moved between the first and second open configurations to the first and second open configurations and the first and second closed configurations.

Abstract: An apparatus for delivering a clip includes an introducer sheath including an outer surface extending between its proximal and distal ends. A clip is carried on the outer surface, e.g., on a carrier assembly that is slidable along the outer surface from the proximal end towards the distal end. A skin overlies the outer surface of the sheath and the carrier assembly that is separable from the outer surface as the carrier assembly is advanced from the proximal end towards the distal end of the sheath. During use, the distal end of the sheath is inserted into an opening through tissue, e.g., into a puncture communicating with a blood vessel. The carrier assembly is advanced towards the distal end of the sheath, causing the skin to separate from the outer surface of the elongate member, and the clip is deployed from the carrier to seal the opening.

Abstract: A spinal device for carrying out a surgical procedure on vertebrae by a posterior or posterolateral approach, including at least one tube, at least one spinal screw capable of engaging with the proximal end of a tube, wherein the device also comprises a connection accessory, having means of reversible fastening to at least one of said tubes, said connection part being configured such as to keep at least one of said tubes in an open angular position.

Abstract: A retractor system for use in spinal surgical procedures includes at least two retractor blades, each of the at least two retractor blades, a shim and a shim inserter. The shim has an expansion band and the shim inserter is configured to slide the shim between and along the at least two retractor blades and dispose the shim at a distal end of the at least two retractor blades. The shim spreads the at least two retractor blades away from each other when the shim insert slides the shim between and along the at least two retractor blades and the shim prevents the distal end of each of the at least two retractor blades from closing in on each other due to musculature load when the shim is disposed at the distal end of the at least two retractor blades.

Abstract: A system for treating a prostate includes a cartridge, a handle configured to receive the cartridge, and an anchor assembly. The cartridge includes the anchor assembly and the handle includes an actuator and a spring mechanism loaded with mechanical energy. The cartridge and handle mate via pivoting and are aligned via alignment features.

Abstract: A suture anchor including an outer anchor part and an inner anchor part. The outer anchor part includes a proximal end, a distal end, and an inner surface defining a center bore extending between the proximal end and the distal end. The center bore includes a tapered proximal portion. The inner anchor part includes a tapered outer surface defining a first pair of opposing apertures. Insertion of the inner anchor part into the tapered proximal portion of the outer anchor part enables a suture extending through the first pair of opposing apertures to be coupled to the suture anchor. A taper fit between the tapered proximal portion of the center bore of the outer anchor part and the tapered outer surface of the inner anchor part retains the inner anchor part within the outer anchor part.

Abstract: Systems and methods are provided for suturing tissue. An elongated deployment shaft carries a needle deployment assembly with needles carrying suture material. A needle catcher is disposed over the shaft and configured to engage and retain at least a portion of each of the needles carrying the suture material when the needles are passed through the tissue to be sutured to a proximal position.

Abstract: A guide member configured for guiding a suture passer through a cannula and tissue surrounding the cannula to facilitate closure of an opening in tissue. The guide member includes a guide housing and an elongated guide shaft. The guide housing is configured for releasably engaging the guide member with the cannula and defines an entry aperture. The elongated guide shaft extends distally from the guide housing and defines an annular exterior surface. An exit aperture is defined through the annular exterior surface. The guide member defines a lumen extending from the entry aperture, through the guide housing and the elongated guide shaft, to the exit aperture. The entry aperture, lumen, and exit aperture cooperating to define a passageway extending through the guide member.

Abstract: A loading unit for a surgical stapling device has a cartridge assembly and an anvil assembly, the cartridge assembly including a channel and a staple cartridge having a plurality of surgical staples therein. An axial drive assembly has a clamping member, the clamping member having an upper flange for engaging the anvil assembly, and a lower flange for engaging the channel. The axial drive assembly is movable through the staple cartridge to drive the staples out of the staple cartridge and against the anvil assembly. Mechanical features are defined in the channel for indicating an end of stroke for the axial drive assembly, the mechanical features having a first pattern and a second pattern.

Abstract: An apparatus includes a body, a shaft assembly, an end effector, and a staple cartridge. The end effector includes an anvil and a lower jaw. The anvil is pivotable toward the lower jaw to clamp tissue. The staple cartridge is coupled with the lower jaw. The staple cartridge includes a deck, a plurality of staples, and a plurality of staple drivers. The deck faces the anvil. The staples are positioned in a plurality of staple openings formed through the deck. The staple drivers are configured to drive the staples out of the staple openings. Each staple driver of the plurality of staple drivers includes a staple driver body. At least a portion of the staple drivers further include a compressible feature extending from the staple driver body toward the anvil.

Abstract: A surgical instrument system can comprise a surgical instrument for use with a loading unit comprising an end effector, wherein the loading unit is releasably attachable to the surgical instrument. The surgical instrument comprises a motor configured to drive a firing member and is configured to determine whether the loading unit includes a datum identifying the loading unit or is otherwise identifiable. If the loading unit is identifiable, then the motor of the surgical instrument fires a first firing rate. If the loading unit is not identifiable, then the motor of the surgical instrument fires at a second firing rate.

Abstract: Described is an inflatable implant suitable for placement in the human body and left there for an indeterminate and potentially lengthy period of time. The implant is one that has a low profile when introduced into the body and a larger profile when it is inflated with one or more filler materials. Depending upon design and use choices the delivered implant may be removable and adjustable in situ in size, position, location, form, and rigidity. Indeed, in some variations, the design of the implant may be such that it may be removed at a potentially fairly lengthy time after implantation. The implant includes at least one bladder wall that generally is at least partially non-elastic (or unexpandable) after the preselected size is reached. The bladder wall will define at least one fillable volume and may form more than one independent fillable volumes. The bladder wall, in some variations, may be partially elastic or expandable to permit adjustment of implant size or configuration after or during delivery.

Abstract: An occlusion system (5) provides a trimmable continuous embolic coil (10) that is “cut to length” at the end of its deployment into the target occlusion site. A delivery device (15) provides the “cut to length” feature for the continuous embolic coil.

Abstract: A medical instrument comprising an end effector comprising a first jaw configured to be repositionable with respect to a second jaw, the first and second jaws removably mounted to an open-ended occlusion clip, the end effector configured to configured to be removably coupled to an open-ended occlusion clip with a pair of terminal ends and first and second robotic arms, and wherein the end effector includes at least one of a cavity and a projection configured to be engaged by at least one of the first and second robotic arms.

Abstract: The ligation clip includes opposing legs connected at a connection point at which the clip pivots to the clamped position on a vessel. The entire clip has a completely semi-circular outside surface. The inside vessel engaging surfaces of the legs of the clip have a unique vessel retaining system that includes a plurality of rounded protrusions alternating with rounded depressions. The retaining system is positioned “within” the inside vessel engaging surfaces of the legs such that a flat surface remains adjacent to our around the retaining system. In addition, there are no sharp edges associated with the ligation clip. All transition points between the outer and inner surfaces of the clip are rounded to prevent any sharp edges.

Abstract: A sleeve for use with a tourniquet cuff to protect a patient's limb from tourniquet-related injury includes a stretchable body extending longitudinally over a sleeve length between a proximal end and a distal end. The body has a tubular shape, and the sleeve length is greater than a width of the tourniquet cuff. The body tapers from the proximal end to the distal end such that a proximal end circumference is greater than a distal end circumference. The body is formed to apply substantially uniform pressure to the patient's limb from the proximal end of the sleeve to the distal end of the sleeve varying only within a predetermined pressure range.

Abstract: Tools adapted for spinal distraction are provided. More specifically, tools having an elongate shaft connected to a head portion are provided for imparting a force for displacing vertebral bodies. The tools may comprise features, such as textured surfaces or the ability to transmit pressure, for cleaning and preparing a spinal disc space for subsequent tools and procedures. A plurality or set of distraction tools is contemplated where the plurality of tools is made up of tools having various distinctions from one another. Such distinctions may be in the way of length, width, angle, and other geometric features or may comprise differences in materials or additional features.

Abstract: Methods and devices for performing knee arthroplasty including but not limited to bicruciate retaining knee arthroplasty are provided. Methods and devices for preparing a proximal tibia for a tibial implant are also provided. These methods and devices, in at least some embodiments and uses, facilitate decreasing the complexity of knee arthroplasty procedures such as bicruciate retaining procedures while maintaining, if not improving on, the safety, accuracy and/or effectiveness of such procedures.

Abstract: A surgical instrument including a customized patient-specific guide block is disclosed. The customized patient-specific guide block includes a first surface, a bone-facing surface, a second surface positioned opposite the first surface and the bone-facing surface, and a guide pin hole extending between the second surface and the bone-facing surface. The first surface has a customized prosthesis-specific negative contour shaped to match a corresponding contour of a prosthetic component, and the customized prosthesis-specific negative contour includes a concave surface shaped to match a convex surface of the corresponding contour of the prosthetic component. A method of performing an orthopedic surgical procedure is also disclosed.

Abstract: Aligning the syndesmosis joint by a novel device and method includes establishing a first plane by attaching a bone plate to the posterolateral aspect of the distal fibula. A second transverse plane arranges perpendicular to the first nominal plane. A syndesmosis targeting guide device includes a post having a post axis extending perpendicular to the first plane and in the second plane. The device includes a curvilinear slider guide extending along an arc in the second plane. The slider is positioned to a first position and fixing that first position to establish a fixed entry point in the fibula wherein the fixed entry point lies in the second plane and further thereby establishing a desired trajectory in the second plane wherein the trajectory includes the fixed entry point based on the slider first position.

Abstract: A method of increasing blood flow through an obstructed blood vessel includes providing an expandable member substantially made of a mesh having a plurality of interstices. The expandable member is inserted into the blood vessel, positioned within the blood vessel with the proximal member end upstream of the distal member end and the member body located radially adjacent at least a portion of an obstruction, and expanded to bring at least a portion of the member body into contact with the obstruction. An outward radial force is exerted on the obstruction to dislodge at least one fragment from the obstruction and to enhance blood flow through the blood vessel past the obstruction. The at least one fragment is passed through at least one interstice of the member body in the radial direction, and is selectively retained within the expandable member.

Abstract: A clot retrieval device may include an elongate shaft and an expandable section. The expandable section may include a framework of interconnected strut elements. The connection region between adjacent strut elements may include crown elements. Additionally, the framework may be formed from a substrate material and at least a portion of a plurality of said strut elements may be coated with a coating material. Further, at least a portion of a plurality of said crown elements may not be coated with said coating material.

Abstract: A device for use in performing minimally invasive surgery. A system for performing minimally invasive surgery comprising the device according to the present invention. A method for performing minimally invasive surgery.

Abstract: A contoured forceps handle is presented having a first arm with a contoured surface and a second arm with a contoured surface to provide for rotation in the hand of a user. The forceps handle may be used with a forceps or may have tips attached. Contoured forceps onlays are also presented that may be attached to forceps.

Abstract: In various embodiments, a surgical instrument system comprising an end effector, an elongate shaft, a motor-powered closure member, and a motor-powered firing system is disclosed. The end effector comprises an anvil and a cartridge channel. The cartridge channel is configured to receive a staple cartridge. The motor-powered closure member is moveable between a first position and a second position during a closure stroke. The motor-powered closure member couples the anvil and the channel during the closure stroke. The motor-powered firing system comprises a first flange configured to engage the anvil during a firing stroke, a second flange configured to engage the cartridge channel during the firing stroke, and a rotatable drive screw operable to transmit the firing stroke. The first and second flanges couple the anvil and the channel during the firing stroke. The motor-powered closure member and the motor-powered firing system are separately actuatable.

Abstract: Various electrical and slip ring connector arrangements configured to facilitate the passage of electrical current and signals between two components that are rotatable relative to each other such as an interchangeable surgical shaft assembly that includes portions that are rotatable relative to fixed mounting portions.

Abstract: Various embodiments described herein are directed to surgical instruments with visual feedback. In one embodiment, a surgical instrument with visual feedback comprises an end effector. The end effector has a first jaw member and a second jaw member. At least one sensor is coupled to the end effector. The at least one sensor is configured convert at least one state of the end effector to a feedback signal. The feedback signal is corresponding to the at least one state of the end effector. The feedback signal may be transmitted to a display to render a visual representation of the at least one state of the end effector. The surgical instrument may further comprise an instrument mounting portion to mount to a robotic surgical system. The instrument mounting portion comprises an interface to mechanically and electrically interface to the surgical instrument.

Abstract: A method for treating cartilage of a human being includes bringing an excision unit which ultrasonically vibrates into contact with a predetermined portion of the cartilage, heating the predetermined portion of the cartilage to a temperature of 120° C. or higher by the excision unit and excising, by the excision unit, the predetermined portion of the cartilage that has been heated to the temperature of 120° C. or higher while pressing the predetermined portion.

Abstract: A tissue collection needle with a hollow interior provides two opposing tips with beveled edges on facets that drive tissue toward the hollow interior where the tissue can be gathered and severed from surrounding tissue as the needle advances through a biological specimen. The points and bevels are advantageously formed from a minimal number of cuts amenable to rapid fabrication from readily available hollow needle stock.

Abstract: A contained tissue extraction device for morcellating a tissue inside an intracorporeal cavity is disclosed. Particularly, the contained tissue extraction device includes serrated-blade wire segments that are sandwiched between an inner bag and an outer bag. The contained tissue extraction device may capture a target tissue such that a surgeon may pull the contained tissue extraction device taught through an incision that is smaller than the target tissue. The contained tissue extraction device allows a surgeon to morcellate the contained tissue by oscillating wire ends of the wire segments back and forth.

Abstract: A scalpel handle sheath includes a body defining a first end and an arm adjacent the first end, the flexible arm having a first boss extending inwardly therefrom and a second boss extending outwardly from the arm. The scalpel handle sheath also includes a shield coupled with the body and slideable between a retracted position and a removal position. The shield defines an edge applying an inward force on the second boss during movement of the shield from the extended position to the removal position and a removal flange extending within the shield and passing the first end of the body during movement of the shield into the removal position.

Abstract: An anti-reverse apparatus includes a latch capable of stopping an end sealing piece from moving reversely, and a loose switch capable of relieving a stop action by the latch on the reverse movement of the end sealing piece. Limitation of the latch on the reverse movement of the end sealing piece can be relieved by pressing the loose switch down. When the end sealing piece is detachably mounted at a near end of a sleeve in a rotating manner, the latch can stop reverse movement causing loosening of the end sealing piece and prevent air leakage or the end sealing piece from loosening from the near end of the sleeve. When the loose switch is pressed down, limitation of the latch on the reverse movement of the end sealing piece can be relieved, and the end sealing piece can be detached from the near end of the sleeve.

Abstract: A port for laparoscopic surgery comprises an opening for attachment to a wound protector and a flexible membrane extending therefrom to define an airtight seal around an incision in a patient. A plurality of access points are defined in the membrane, through which laparoscopic trocars and elongate laparoscopic surgical instruments can be inserted.

Abstract: This disclosure relates to a cannula for a surgical instrument used for cutting selected tissue in a body cavity while under visual inspection. A kit containing the cannula and methods for performing surgical procedures using the cannula are also described.

Abstract: A neuromonitoring needle electrode placement gun which includes a housing, at least a first needle electrode and housing assembly, an elongated channel dimensioned and configured for accommodating axial movement of the at least a first needle electrode and housing assembly within the channel and for directing movement of the at least a first needle electrode and housing assembly and a pusher dimensioned and configured for engaging the at least a first needle electrode and housing assembly and for axially displacing the at least a first needle electrode and housing assembly.

Abstract: An assembly tool for assembling components of an implant can include a finger assembly, a handle assembly, and a crossbar assembly. The finger assembly can include first and second fingers oriented parallel to each other, and sized and shaped to releasably engage first and second components of the implant during assembly. The handle assembly can include first and second handles pivotally connected to each other and configured to control movement of the first and second fingers. The crossbar assembly can be configured to maintain the first and second fingers substantially parallel to each other during movement of the first and second fingers. The assembly tool can be used for assembling a bearing assembly to an ulnar component of an elbow prosthesis.

Abstract: A device for accessing and guiding at least one fixation device to a spine may include a distal portion configured to fit in a facet of the spine and a proximal portion extending from the distal portion. The proximal portion may be detachable from the distal portion and may be hollow or solid. A system for accessing and guiding at least one fixation device to a spine may include a distal portion configured to fit in a facet of the spine, a proximal portion extending from the distal portion, and a slidable guide device for sliding over the facet guide device to guide at least one instrument to the spine.

Abstract: A system, devices and methods are provided for facilitating stabilization of periarticular fractures. The system includes a compression plate and one or more of a cerclage cable for encircling the bone and securing the compression plate to the bone, a crimp lug for securing the cable in tension relative to the bone and/or a plate, and a supplemental plate coupled to the compression plate and adapted to receive bicortical or unicortical bone screws to further secure the compression plate relative to the bone. In addition, the system includes a cable tensioner for temporarily retaining the cable in tension and then applying a tension to the cable until a desired compression is effected between a plate and bone and while a cable retaining structure is secured to the cable to retain the applied tension on the cable. Also provided is a jig for use with plates for minimally invasive fracture stabilization.

Abstract: A method of treating a spinal column shape deformation includes fixing at least two fixation screw assemblies to respective vertebrae, sliding a rod between the arm extensions on each of the fixation screw assemblies, swinging the channels of the screw assemblies relative to the fixation screws so that the channels become less inclined to the axes of the fixation screws, and so that the rod is located generally posteriorly of the spinal column, locking the channel against swinging relative to the screw, rotating the rod about its axis relative to at least one of the channels, and locking the rod against movement relative to the channel.

Abstract: An injection device is provided for repairing biological tissues and comprises a body, a chamber, an exterior tube, and a screw rod. The chamber is connected with the body and used for accommodating a repairing material. The exterior tube is connected with the chamber. The screw rod is disposed inside the chamber and the exterior tube. The threads of the screw rod disperse the repairing material. By using the threads of the screw rod and a driving force originating from the end of the screw rod, the repairing material is delivered into an organism.

Abstract: An apparatus can include a shaft having a mating end and a driving end and having an axial slot; a sliding member located within the axial slot; and an activator to advance the sliding member towards the mating end of the shaft; wherein the axial slot includes a surface proximate the mating end to move a distal end of the sliding member into a retaining position.

Abstract: Treatment systems, methods, and apparatuses for improving the appearance of skin or other target regions are described as well as for providing for other treatments. Aspects of the technology are directed to improving the appearance of skin by tightening the skin, improving skin tone or texture, eliminating or reducing wrinkles, increasing skin smoothness, or improving the appearance of cellulite. Treatments can include cooling a surface of a patient's skin and detecting at least one freeze event in the cooled skin. The treatment system can continue cooling the patient's skin after the freeze event(s) are detected so to maintain at least a partially frozen state of the tissue for a period of time.

Abstract: A surgical instrument for use in laparoscopic surgical procedures is disclosed that includes an elongated shaped outer shaft having opposed proximal and distal end portions, and having a non-circular cross-sectional profile, an end effector operatively associated with a distal end portion of the shaped outer shaft and including a pair of cooperating jaw members configured for movement between open and closed positions, a proximal handle assembly operatively associated with a proximal end portion of the shaped outer shaft and including a pivoting actuation handle, and an elongated actuation member extending through the shaped outer shaft from the proximal handle assembly to the end effector, whereby movement of the actuation handle causes corresponding movement of the cooperating jaw members.

Abstract: A surgical generator is disclosed including an ultrasonic generator module to provide at an ultrasonic drive signal for driving an ultrasonic surgical device and an electrosurgical generator module to provice an electrosurgical drive signal for driving an electrosurgical device. At least one of providing the ultrasonic drive signal or providing the electrosurgical drive signal includes recalling a waveform sample from a look-up table (LUT), modifying the waveform sample to generate a modified waveform based on voltage and current feedback information to pre-distort the waveform sample on a dynamic ongoing basis, indexing each stored voltage and current feedback data pair based on a corresponding LUT sample that was output when the voltage and current feedback data pair was acquired, synchronizing the LUT sample and the voltage and current feedback data pair to correct timing and stability of the pre-distorted waveform sample, and providing the modified waveform to an output stage.

Abstract: An apparatus comprises a first longitudinal member and a second longitudinal member configured to be located near a tissue region. An energy source is coupled to first longitudinal member and second longitudinal member. A measuring device is configured to measure at least one characteristic of the tissue region. An energy controller is coupled to the energy source and the measuring device. The energy controller includes a processor coupled to a memory and configured to execute programmed instructions stored in the memory, comprising initiating a delivery of energy to the tissue region from the energy source. One or more items of data are received from the measuring device based on the delivery of energy to the tissue region. The delivery of energy to the tissue region is adjusted based on the one or more items of data.

Abstract: A bipolar electrosurgical instrument includes first and second shafts each having a jaw member extending from its distal end. Each jaw member is adapted to connect to a source of electrosurgical energy such that the jaw members are capable of selectively conducting energy through tissue held therebetween. A knife channel is configured to reciprocate a cutting mechanism therealong. An actuator selectively advances the cutting mechanism. A switch is disposed on the first shaft and is configured to be depressed between a first position and at least one subsequent position upon biasing engagement with a mechanical interface disposed on the second shaft. The first position of the switch relays information to the user corresponding to a desired pressure on tissue and the at least one subsequent position is configured to activate the source of electrosurgical energy to supply electrosurgical energy to the jaw members.