Abstract: A knife member that can have a blade portion configured operation within a surgical stapling device. A first frame portion can extend from the blade portion to a first connection portion. A second frame portion can extend from the first frame portion to a second connection portion. At least one of the first and second frame portions can include a fused portion. The fused portion can be configured to fail when a predetermined amount of force is applied to the fused portion.

Abstract: A surgical stapling apparatus is disclosed which comprises a tissue stop configured to inhibit tissue from flowing out of the distal end of the stapling instrument as the tissue is being stapled and/or incised. Also disclosed is a surgical stapling apparatus comprising one or more interruptions, or absent staple cavities, in the rows of staple cavities defined therein. Also disclosed is a surgical stapling apparatus comprising a channel configured to receive tissue and/or another surgical instrument therein. In at least one instance, such a stapling apparatus could comprise staple cavities on one side of a longitudinal knife slot and no staple cavities on the other side of the knife slot. Further disclosed are methods for using the surgical stapling devices disclosed herein.

Abstract: A surgical stapling device that comprises an end effector that is configured to receive various control motions from a robotic system.

Abstract: A process and system are disclosed for downloading sensor data, stored in a memory device of a surgical cutting and fastening instrument, to an external or remote computer device. The process may involve storing data from one or more sensors of a surgical cutting and fastening instrument in a memory device of a control unit of the surgical cutting and fastening instrument during a surgical procedure involving the surgical cutting and fastening instrument. Next, after the surgical procedure, a data link between the control unit and the remote computer device is established. Then, the sensor data can be downloaded from the control unit to the remote computer device.

Abstract: A surgical instrument includes a shell assembly and an adapter. The shell assembly includes a shell housing, a plurality of staples, a staple pusher configured to eject the plurality of staples from the shell housing, a staple actuator configured to engage the staple pusher, a knife member, and a knife carrier supporting the knife member. The adapter includes a staple band operatively coupled to an actuation mechanism for axial displacement, a knife band at least partially received within the staple band, and a cam ring rotatably supported about the knife band. The staple band is configured to releasably engage the staple actuator. The knife band is operatively coupled with an actuation mechanism for axial displacement. The cam ring is rotatable between an engaged position in which the knife carrier engages the cam ring for concomitant axial displacement with the knife band and a disengaged position in which the knife carrier is disengaged from the cam ring.

Abstract: A surgical device includes an actuator assembly including a handle, an adapter assembly extending distally from the adapter assembly, and a tool assembly supported on a distal portion of the adapter assembly. The adapter assembly includes a rotation assembly that rotatably supports the adapter assembly in relation to the actuator assembly and a wire harness that allows the actuator assembly to communicate with the tool assembly. The rotation assembly includes a stop assembly for limiting a degree of rotation of the adapter assembly in relation to the actuator assembly to prevent separation of the wire harness from communication with the actuator assembly and/or the tool assembly. The stop assembly includes a stop plate and a stop pin that are spaced from the wire harness to minimize the likelihood of damage to the wire harness during rotation of the adapter assembly in relation to the actuator assembly.

Abstract: An occlusion clamp including: (a) an occlusion tongs including a primary spring coupling a first longitudinal arm to a second longitudinal arm, the first longitudinal arm including a first linear occlusion surface configured to be parallel to and overlap a second linear occlusion surface of the second longitudinal arm, each of the first and second longitudinal arms having a free distal end; and, (b) a secondary spring removably coupled to the occlusion tongs.

Abstract: A rectal band ligation device and a method of operating the band ligation device. In one embodiment, the band ligation device includes: (1) a handle having a trigger associated therewith, (2) an extension tube extending from the handle and terminating in a head, (3) at least two openings in the head, (4) hollow pistons located in the openings and configured to move relative thereto between an extended position in which ends of the pistons are exposed through the openings and a retracted position, gaps between corresponding openings and hollow pistons being less than cross-sectional widths of elastic members stretched around the ends and (5) an actuating rod coupling the trigger and the pistons and configured to cause the pistons to move from the extended position to the retracted position.

Abstract: A device for delivering an implant (e.g., an embolic micro-coil) to a vascular disorder of a patient includes a delivery pusher, a moveable element, and first and second elongate members. The delivery pusher defines a lumen between its proximal and distal ends. The moveable element (e.g., a floating tube or a floating coil) defines a passageway therethrough and is disposed within the lumen of the delivery pusher. The first and second elongate members (e.g., core wires) are also disposed within the lumen of the delivery pusher. A portion of each elongate member passes through the passageway of the moveable element. Movement of the first elongate member in a first direction (e.g., retraction of the first elongate member from a locked to an unlocked configuration) causes a time-delayed or lost motion movement of the second elongate member in the same (i.e., first) direction, which releases the implant from the delivery pusher.

Abstract: This invention relates to an aneurysm occluder, and more particularly but not exclusively, to an endovascular aneurysm occluder that can be inserted into an aneurysm cavity by using endovascular surgical procedures. The aneurysm occluder has a deformable housing (2) and an absorber (8) or material that causes blood clotting made of an absorbent material in an/or attached to the housing.

Abstract: An expansile member that may be used on a delivery device or may be used for occlusive purposes within the vasculature.

Abstract: Endoscopic reposable surgical clip appliers including a reusable handle assembly and at least one reusable shaft assembly.

Abstract: A reposable surgical clip applier includes a handle assembly, a shaft assembly releasably engagable with the handle assembly, and a clip cartridge assembly releasably engagable within the shaft assembly. When the reposable surgical clip applier is assembled, a proximal drive of the handle assembly is positioned proximally adjacent an inner drive of the shaft assembly such that movement of handle(s) of the handle assembly towards an approximated position actuates a jaw assembly of the shaft assembly. When the reposable surgical clip applier is assembled, a proximal pusher of the handle assembly is positioned proximally adjacent a distal pusher of the clip cartridge assembly such that movement of the handle(s) towards a spaced-apart position loads a distal-most surgical clip from the clip cartridge assembly into the jaw assembly.

Abstract: A device and method to occlude blood flow through a subclavian artery and subclavian vein is presented. Small incisions are formed both superior and inferior to the clavicle. A closure element is introduced into one incision, passed posterior to the clavicle and vessels, and withdrawn through a second incision, such that a first end of the closure element extends from one incision and the second end extends from the other incision. The closure element is formed into a closed loop around the clavicle and vessels. The loop is tightened to occlude blood flow through the vessels. Locking features on the closure element enable rapid and secure cinching of the loop. A second closure element may be delivered through the same pathway and used for enhanced stability of the occlusion. A delivery member may be used to carry the closure element(s) through the incisions.

Abstract: This invention relates to an aneurysm occluder, and more particularly but not exclusively, to an endovascular aneurysm occluder that can be inserted into an aneurysm cavity by using endovascular surgical procedures. The aneurysm occluder, includes a resiliently deformable cage (2) made of a mesh structure in which the mesh structure is cylindrical in cross section and closed off at opposite ends, where the opposite ends are held and closed off with shanks (4).

Abstract: A catheter system for treating lesions is provided. The system is suitable for treatment of bifurcation lesions, has a low profile and provides substantially predictable translational and rotational positioning. In one embodiment, the system includes a fixed wire balloon catheter and a partially attached guidewire lumen, wherein the guidewire lumen is attached to the catheter at a crotch point. The location of the crotch point is predetermined so as to provide substantially predictable positioning. Several embodiments of the system are described for various types of lesions and vessel configurations.

Abstract: The disclosure sets forth various exemplary embodiments of systems, methods, and/or medical apparatuses including but not limited to: a sheath; and a balloon disposed at a working distal end of the sheath. According to one example embodiment the medical device can include where the sheath can include woven wire reinforcing axial and longitudinal strength, side holes, a one direction distal valve, and can include an inflator. According to one example embodiment the medical device can include where the sheath can include a narrow cross-section of, e.g., 7-8 Fr and balloon of length of, e.g., 12 cm.

Abstract: Devices and methods comprising hybrid implants for occluding endovascular and non-endovascular defects are disclosed, including parent artery occlusions, aneurysms, and other abnormal openings in the body.

Abstract: The present invention teaches the use of a disc shaped mesh intrasaccular occlusion structure with at least one hole in said disc, with optional supplemental hydrogel, which is designed to implement an endovascular treatment to facilitate saccular aneurysm treatment while ameliorating or eliminating aneurysm recurrence.

Abstract: A tourniquet with an attached timer. The tourniquet includes a main strap. The main strap is an elongated strap having a first end opposite a second end, and an upper surface opposite a lower surface. The timer is attached to the main strap. The timer is used to keep track of the amount of time the tourniquet is applied to the user.

Abstract: The present disclosure relates to a saw, comprising a drive, a first blade configured to oscillate about an axis perpendicular to a plane defined by a surface of the first blade, a second blade configured to oscillate about an axis perpendicular to the plane in a direction opposite to that of the first blade, and wherein gearing is provided between the drive and the first and second blades to reduce the speed transmitted from the drive to the blades. A saw blade, a connection mechanism for connecting a blade to a saw and associated methods are also provided.

Abstract: A number of orthopaedic surgical instruments are also disclosed. A method, apparatus, and system for fabricating such instruments are also disclosed.

Abstract: A cannula tool in combination with other tools is used to provide multiple instruments necessary for surgical procedures. The cannula tool is used in combination with a piercing tool to form a dilator instrument to access a treatment site and in combination with a plunger tool to deliver biological or grafting material to a treatment site. Each of the plunger and piercing tools includes a guide lumen to track the tools over a K-wire or other guide device for placement at the treatment site. The application discloses asymmetrical piercing and plunger tools for placement proximate to a facet joint for treatment.

Abstract: A surgical instrument includes a first member defining an axis and including a cutting surface. A second member includes a cutting surface that is rotatable relative to the first member. A third member includes an outer surface. The cutting surface of the second member is rotatable relative to the outer surface to transfer the cut tissue along the axis. Systems and methods are disclosed.

Abstract: A system for establishing an intramedullary path includes a body sized and configured to be received within a resected bone space. The body defines a first aperture that extends through the body and is sized and configured to receive a surgical tool therethrough. A first bone engaging structure extends from the body in a first direction and includes a first surface that is complementary to a surface topography of a first bone. When the first surface of the bone engaging structure engages the surface topography of the first bone to which the first surface is complementary, an axis defined by the first aperture is substantially collinear with a mechanical axis of the first bone.

Abstract: The present invention provides a drill guide for orthopedic surgery. The drill guide is configured to facilitate drilling of a bone tunnel with a correct and repeatable placement. The drill guide is designed for drilling of the femoral bone during knee surgery. More particularly, in certain embodiments the drill guide is designed for ACL repair and replacement surgery. In a preferred embodiment of the present invention, the guide has 5 members: a center rail, a side rail, an anteromedial slider, a femoral slider, and a center pin.

Abstract: A wedge osteotomy method inserts a first wire into a first bone of the foot, distal from tissue to be removed. A second wire is inserted into a second bone, so the tissue to be removed is distal from the second wire. A cut guide is pivoted about the first wire, until a first axis of the cut guide is parallel with a longitudinal axis of the first metatarsal. The cut guide has a slot perpendicular to the first axis for guiding a cutter to cut bone, while the first axis is aligned with the longitudinal axis of the first metatarsal. The cut guide is then pivoted about the second wire, until the first axis is aligned with the longitudinal axis of the talus, and bone is cut through the slot, to form a second planar cut into or through bone material.

Abstract: Methods for collapsing a tubular organ, such as the esophagus, involve inserting a device into the tubular organ, at least partially sealing off a section of the tubular organ, and drawing in the wall of the tubular organ by application of suction. The devices may be used to move the wall of the tubular organ away from an area undergoing treatment or therapy, such as to minimize damage to the tubular organ by application of radiofrequency energy or to limit temperature increase of the tubular organ.

Abstract: A method for treating tissue of at least one of an internal carotid artery, an ophthalmic artery, or an ostium between the internal carotid artery and the ophthalmic artery of a subject may include expanding a first expandable device of a first device in the internal carotid artery. The method also may include delivering a second device in the ophthalmic artery via the first device and expanding a second expandable device of the second device in the ophthalmic artery. Further, the method may include adjusting a radial position of the second expandable device relative to the first expandable device.

Abstract: An endoscope treatment tool includes: a sheath having a lumen; a basket section protruding from the lumen and having an elastic wire; and an operating wire. The elastic wire has: a maximum section where the outer diameter of the basket section is largest of the elastic wire; a first section that, in a lateral view from a direction orthogonal to a normal from the maximum section to the central axis of the basket section, is largest on the opposite side of the central axis from the maximum section between the maximum section and the proximal end; and a second section that is largest at a position away from the normal between the maximum section and the first section, and in the front view, the first section is located on the opposite side of a straight line orthogonal to the normal at the central axis from the maximum section side.

Abstract: A system for breaking obstructions in body lumens includes a catheter including an elongated carrier, a balloon about the carrier in sealed relation thereto, the balloon being arranged to receive a fluid therein that inflates the balloon, and an arc generator including at least one electrode within the balloon that forms a mechanical shock wave within the balloon. The system further includes a power source that provides electrical energy to the arc generator.

Abstract: Membrane forceps for performing an ILM or ERM peel procedure include a handle, a tube extending from the handle, and forceps jaws extending from the tube. The forceps jaws may be configured to grasp an ILM or ERM, and may include an outer surface having a roughened surface. The roughened surface may be structurally configured to aid in gaining an edge of the ILM or ERM.

Abstract: In one embodiment, a vacuum-actuated surgical grasper includes a suction head adapted to interface with patient tissue, a suction tube connected to and in fluid communication with the suction head, and a handle connected to the suction tube, the handle comprising an internal passage in fluid communication with the suction tube through which fluid from the suction tube can flow and a pivotable actuation lever that controls this flow through the passage.

Abstract: A steerable guidewire. The steerable guidewire is fabricated includes an outer tube, an inner tube, a hub, and a distal articulating region. The steerable guidewire hub can be removed to permit advancement of catheters over its proximal end followed by re-attachment of the hub to permit deflection of the distal end of the steerable guidewire.

Abstract: An ultrasound transducer assembly includes an acoustic focusing lens and a therapy transducer mounted to a holder member so that the lens is movable relative to the transducer. The lens and the transducer are mounted to the holder member so that the lens is spaced a predetermined distance from the transducer element. A liquid layer having a thickness of the predetermined distance is provided between the lens and the transducer element. A solid backing member is disposed on a side of the transducer element opposite the lens. The backing member is spaced by an additional liquid layer of a predetermined thickness from the transducer element. The focusing depth of the lens—transducer assembly is controllable by transducer operating frequency.

Abstract: A medical device includes: the vibration transmission member; a first cross-sectional area reduction portion, which makes a cross-sectional area of a distal end portion concerning a plane intersecting with a central axis of the vibration transmission member smaller than a cross-sectional area of the intermediate portion; and a second cross-sectional area reduction portion which makes a cross-sectional area concerning a plane intersecting with the central axis of a half portion of the vibration transmission member located opposite to the first cross-sectional area reduction portion smaller than a cross-sectional area of a half portion of the vibration transmission member located closer to the first cross-sectional area reduction portion.

Abstract: A tissue-removing catheter for removing tissue in a body lumen includes an elongate body and a handle mounted to a proximal end portion of the elongate body. The handle is operable to cause rotation of the elongate body. A tissue-removing element is mounted on a distal end portion of the elongate body. The tissue-removing element is configured to remove the tissue as the tissue-removing element is rotated by the elongate body within the body lumen. An inner liner is received within the elongate body and is coupled to the handle at a proximal end portion of the inner liner. The inner liner defines a guidewire lumen. The inner liner is coupled to the tissue-removing element at a distal end portion of the inner liner such that translational movement of the inner liner in the body lumen causes a corresponding translational movement of the tissue-removing element.

Abstract: A tissue-removing catheter for removing tissue in a body lumen includes an elongate body. A tissue-removing element mounted on a distal end portion of the elongate body. The tissue-removing element includes a body including an exterior surface having a first segment extending from a proximal end toward a distal end of the tissue-removing element. A second segment extends from the first segment toward the distal end of the tissue-removing element. A third segment extends from the second segment to the distal end of the tissue-removing element. A transition between the first and second segments defines a first angle formed between the first and second segments. A transition between the second and third segments defines a second angle formed between the second and third segments. The tissue-removing element is configured to remove the tissue as the tissue-removing element is rotated by the elongate body within the body lumen.

Abstract: A tissue-removing catheter for removing tissue in a body lumen includes an elongate body and a tissue-removing element mounted on a distal end portion of the elongate body. The tissue-removing element is configured to remove the tissue as the tissue-removing element is rotated by the elongate body within the body lumen. An inner liner is received within the elongate body and coupled to a handle at a proximal end of the inner liner. The inner liner defines a guidewire lumen. The inner liner isolates an interior of the guidewire lumen from the elongate body and tissue-removing element such that rotational and torsional forces are not transferred from the elongate body and tissue-removing element to the interior of the guidewire lumen when the elongate body and tissue-removing element are rotated during operation of the tissue-removing catheter.

Abstract: A tissue-removing catheter for removing tissue in a body lumen includes an elongate body sized and shaped to be received in the body lumen. A handle is mounted at a proximal end portion of the catheter and is operable to cause rotation of the elongate body. A tissue-removing element is mounted on a distal end portion of the elongate body. The tissue-removing element is configured to remove the tissue as the tissue-removing element is rotated by the elongate body within the body lumen. A guidewire lumen extends through the elongate body from a distal end of the catheter to an intermediate location on the catheter spaced distally from the proximal end portion of the catheter. The guidewire lumen is configured to receive a guidewire such the catheter can be removed from the body lumen by pulling the catheter along the guidewire without removing the guidewire from the body lumen.

Abstract: A tissue-removing catheter for removing tissue in a body lumen includes an elongate body having an axis and proximal and distal end portions spaced apart from one another along the axis. The elongate body is sized and shaped to be received in the body lumen. A handle is mounted to the proximal end portion of the elongate body and operable to cause rotation of the elongate body. A tissue-removing element is mounted on the distal end portion of the elongate body. An inner liner is received within the elongate body and coupled to the handle at a proximal end of the inner liner. A sensor is arranged with respect to the elongate body and inner liner and is configured to detect wear of the inner liner caused by the elongate body contacting the inner liner during use.

Abstract: An arthroscopic or other surgical cutter has features which facilitate fabrication by ceramic molding. The arthroscopic cutter includes a cutter body having a longitudinal axis and a window, an interior channel, and a plurality of cutting edges extending radially outwardly from an outer surface thereof. The features include non-helical, longitudinally aligned cutting edges, controlled thicknesses of the cutting edges, controlled heights of the cutting edges, controlled areas of the windows, controlled diameters of the internal channels, controlled rake angles of the cutting edges, and other parameters.

Abstract: A method of manufacturing an optical obturator includes providing an injection mold including a mold cavity defining an outer surface of the optical obturator and a core pin centrally positioned within the mold cavity. The core pin defines an inner surface of the optical obturator. In particular, the core pin may be cantilevered to the injection mold. The method further includes injecting a first material between the core pin and the mold cavity to form the tubular shaft and injecting a second material between a distal portion of the core pin and a distal portion of the mold cavity to form the optical tip.

Abstract: The present invention relates to a method for the manufacture of cannulae, as well as cannulae that have been manufactured using the method. The invention further relates to a device that is suitable for the manufacture of cannulae using the method. The method involves the manufacture of a cannula from a hollow tubular segment (1), with a penetrating entity that has a leading penetrating section and a trailing aperture section, wherein the leading penetrating section has a beveled surface that extends rearward from a penetrating tip and has inner lateral edges, and wherein the trailing aperture section has a beveled surface that extends rearward from the beveled surface of the leading section and has inner lateral edges as well as a rounded trailing edge (10, 12), wherein the rounding of trailing edge (10, 12) is produced by means of electrochemical machining (ECM) in the presence of an electrolyte.

Abstract: The present disclosure teaches a novel medical device and method of use, employing a unique shape that allows the device to use the lesser (inferior) curve of aortic Arch as a fulcrum of support for a guide catheter, for subsequent prevention of recoil and displacement thereof, while delivering additional catheters or devices into the distal branches of the great vessels. A method for using same.

Abstract: A seal assembly including a septum seal, a lower seal support, an upper seal support and a return spring is disclosed. The septum seal includes an orifice and a plurality of apertures. The lower seal support includes an engagement surface configured to engage a portion of the septum seal. The upper seal support includes a plurality of fingers, wherein each of the plurality of fingers is configured to extend through a corresponding aperture of the septum seal. The return spring includes a collar portion and a plurality of spokes extending radially outward from the collar portion. At least a portion of the return spring may be sandwiched between the lower seal support and the upper seal support. The plurality of spokes is configured to bias the seal assembly toward a radial center of a housing.

Abstract: Therapeutics and methods of treatment to repair, preserve and grow cartilage are presented. In addition, systems and methods for delivering a therapeutic to a hard to reach anatomical area, such as, for example, the BCI, are presented. A cannulated delivery device provided with a cutting tip, cutting flutes and threads on its distal end can be provided. Using such an exemplary device, various novel therapies for joint and cartilage repair, preservation and generation can be implemented. Alternatively, for disc repair, a delivery device directed to percutaneous intradiscal annular repair, or “PIARES” device can be used to introduce therapeutics intradiscally. The device may have two-needles, with a first cannula/needle, with a finger grip at its distal end, and a longer inner needle to penetrate through the outer needle into the disc, and introduce therapeutics, for example, via a syringe.

Abstract: A system and method are provided to monitor performance of an intraosseous device by using a supporting structure and an attachment mechanism. The attachment mechanism releasably secures the supporting structure proximate an insertion site for the intraosseous device. The supporting structure includes an opening formed therein and sized to receive at least a portion of the intraosseous device. A sensor detects parameters associated with providing fluids and/or medications through the intraosseous device to the bone marrow. The attachment mechanism and the supporting structure cooperate with each other to minimize movement of the intraosseous device relative to the insertion site when the portion of the intraosseous device is disposed in the opening of the supporting structure.

Abstract: A surgical instrument includes: an end effector; a power source; a motor coupled to the power source, the motor configured to actuate the end effector; and a controller operatively coupled to the motor and configured to control the motor based on a current draw of the motor and an angular velocity of the motor.

Abstract: A device includes a plurality of rings. Each ring has a first face, a second face, and at least one slot defined by first and second interior edges of the ring on opposing sides of the slot. The at least one slot penetrates from the first face to the second face. The first face of each ring has a first recess adjacent the slot on the first edge and a second recess adjacent the slot on the second edge. A plurality of posts join each one of the plurality of rings to an adjacent one of the plurality of rings.