Abstract: A blood vessel access closure device includes an inner blood vessel wall support member and an outer blood vessel wall support member. The closure device also includes a deployment member and an electrode. The deployment member is configured to draw the inner and outer blood vessel wall support members towards each other when the inner and outer blood vessel wall members are deployed on opposite sides of a blood vessel wall during closure of a hole in the blood vessel wall. The electrode is configured to be attached to the deployment member and configured to be used to measure impedance.

Abstract: A retractor system for enabling access to a surgical site is disclosed. The retractor system may include a primary retractor assembly configured to open and close a first arm and a second arm along a first path of travel. The primary retractor assembly may include a handle assembly having first and second handles configured to open and close the first and second arms, and the first and second arms may be operably coupled to first and second blades, respectively. The retractor system may further include a secondary retractor assembly configured to couple and uncouple with the primary retractor assembly and independently extend and contract a third arm and optionally a fourth arm. The third arm and optional fourth arm may be operably coupled to third and fourth blades, respectively. The inclination of each blade may be independently adjusted and each arm may also be independently moved.

Abstract: A surgical tissue connector system for moving a first internal body tissue to a position away from a second internal body tissue and then holding the first internal body tissue in the position. Tissue connectors are secured to cords such that the length of cord between the tissue connectors can be easily adjusted in a laparoscopic work space.

Abstract: A simple, threaded suture anchor is pre-loaded with suture in a configuration that allows a surgeon to compress tissue against the bone without tying a knot. The knot-tying step is replaced by a simple suture looping step which requires less time and is not prone to errors in knot tying technique. The suture anchor is a screw-in style anchor body. The suture is loaded into the anchor in a configuration that allows it to create a loop on top of the tissue after it has been passed through the tissue from bottom to top. The suture limbs are then loaded into a knotless anchor which is implanted off the lateral edge of the tissue. Tensioning of the suture limbs in the knotless anchor tightens the loop on top of the tissue, providing a fulcrum point of fixation over the pre-loaded suture anchor without the otherwise need for requisite knot tying.

Abstract: A process for treating a heart valve involves delivering first and second working catheters to a ventricle of a heart of a patient using a transcatheter procedure, approximating a first pad associated with the first working catheter to a backside of a first papillary muscle of the ventricle, approximating a second pad associated with the second working catheter to a backside of a second papillary muscle of the ventricle, and manipulating one or more sutures physically coupled to at least one of the first and second pads to decrease a distance between the first and second papillary muscles.

Abstract: A wound closure device can be provided as described herein. In an example, the wound closure device includes a first suture segment having a first suture configuration and a second suture segment having a second suture configuration. The first and second suture configurations can be different from each other. For example, the first suture configuration can includes a first set of characteristics such as barbed or non-barbed, barb sizes, filament sizes, colors, materials, and/or the like and the second suture configuration can include a second set of characteristics such as barbed or non-barbed, barb sizes, filament sizes, colors, materials and/or the like that can be different from the first set of characteristics. The wound closure device can further include connecting section configured to provide a transition from the first suture segment to the second suture segment.

Abstract: An active anvil assembly for use in forming a looped suture is provided. The active anvil assembly includes an anvil member, a first sensor operably connected to the anvil member, and a control assembly. The first sensor is configured for measuring at least one of force, torque, and distance feedback. Also provided are systems and methods for forming a looped suture including an active anvil assembly.

Abstract: A method of making a surgical suture having a reformed tip includes providing an elongated fiber having a first end, a second end, a central axis extending between the first and second ends thereof, and an outer surface that defines a cross-sectional dimension of the elongated fiber, and compressing a center region of the elongated fiber that is located between the first and second ends thereof for reshaping the center region into a core mass and a deformed mass that extends laterally outside the cross-sectional dimension of said elongated fiber. The method includes separating the deformed mass of the center region from the core mass of the center region so that only the core mass remains for interconnecting the first and second ends of the elongated fiber, and after separating the deformed mass from the core mass, reshaping the core mass into a reformed mass having a reformed mass central axis that is offset from the central axis of the elongated fiber.

Abstract: A device for securing an article to a tissue may include a body, transitionable from a deployment state to a securing state, having a first portion, a second portion, and a medial portion therebetween. The first portion and the second portion may each have an end configured to pierce the tissue. The device in the deployment state may have a linearly extended or a U-shaped structure. In the securing state, the first portion may be embedded in the tissue and the medial portion may contact the article. A system for securing the article to the tissue may releasably engage the device while in the deployment state. A method for securing the article may include contacting the article with a tissue surface and releasing the device from the system so that the device, in the securing state, may anchor the article to the tissue.

Abstract: A device including smart sensors with a local signal processor is disclosed. The device includes an end-effector including at least one sensor and a signal processing component corresponding to the at least one sensor; and a handle configured to receive processed information from the signal processing component. The processed information is generated by the signal processing component at the end-effector based on data received from the at least one sensor at the end-effector.

Abstract: A surgical stapling device includes a tool assembly having an actuation sled assembly that includes an actuation sled and a knife movably supported on the actuation sled. The tool assembly includes structure for moving the knife in relation to the actuation sled between extended and retracted positions in response to movement of the actuation sled through a staple cartridge of the tool assembly. Movement of the knife moves a cutting edge of the knife in relation to the actuation sled within a tissue gap defined by the tool assembly to impart a degree of vertical motion to the cutting edge of the knife. This enables the tool assembly to leverage micro-serrations on the cutting edge of the knife to enhance cutting efficiency of the knife.

Abstract: A surgical stapler includes a first half having a first elongate member and a surface with staple forming pockets. The stapler also includes a second half for releasably coupling with the first half and including a second elongate member having a distal portion for deploying staples. The elongate members are pivotable relative to each other about a pivot axis when the halves are releasably coupled. The stapler further includes a latching member for selectively clamping the halves in a clamped state. The stapler also includes a detent member extending laterally from one of the halves toward the other. The stapler further includes a shoulder member positioned on the other of the halves and configured to selectively engage the detent member in response to rotation of the first elongate member away from the second elongate member to an open state in which the elongate members assume a maximum angular orientation.

Abstract: A surgical apparatus includes an end effector configured to interact with a tissue during a plurality of zones of operation. The surgical apparatus further includes at least one drive mechanism operable to effect at least one motion in the end effector during each of the zones of operation. The surgical apparatus also includes one or more vibration sensors configured to record vibrations generated by the at least one drive mechanism during the zones of operation, wherein the one or more vibration sensors are configured to generate an output signal based on the sensed vibrations, and wherein the output signal is employed to determine a status of the surgical apparatus based on predetermined threshold values that are unique to each of the zones of operation.

Abstract: A surgical stapling system comprising a housing, an end effector, a replaceable staple cartridge, a driver element, a motor-powered firing element, a remote user-controlled console, and a retraction assembly is disclosed. The end effector comprises a first jaw and a second jaw. The first jaw is rotatable relative to the second jaw into a closed position. The driver element is translatable distally in response to a firing motion. The motor-powered firing element is advanceable from a proximal position to a fired position to apply the firing motion to the driver element. The motor-powered firing element is retractable from the fired position toward the proximal position. The remote user- controlled console is capable of controlling the actuation of the motor-powered firing element. The remote user-controlled console comprises apparatus for sensing the closure of the first jaw and apparatus for sensing the advancement and retraction of the motor-powered firing element.

Abstract: A system is disclosed. The system can comprise a replaceable staple cartridge comprising a plurality of staples, a proximal laterally-protruding lug, and a distal laterally-protruding lug. The system can further comprise a channel configured to receive the replaceable staple cartridge, wherein the channel comprises a sidewall comprising a proximal receptacle positioned and dimensioned to receive the proximal laterally-protruding lug and a distal receptacle positioned and dimensioned to receive the distal laterally-protruding lug.

Abstract: A surgical device comprising a first jaw member, a second jaw member, a clamping member and a clamp apparatus is disclosed. The clamping member is slidably positioned to translate at least partially through the first jaw member. The clamping member engages the first jaw member and the second jaw member, and has a knife blade for cutting tissue. A flange of the clamping member is configured to engage a cam surface to pivot the second jaw member with respect to the first jaw member from an open position toward an approximated position. The clamp apparatus is movable from a retracted position to an advanced position for preventing a gap between proximal portions of the first jaw member and the second jaw member from exceeding a predetermined distance. The clamping member and the clamp apparatus are separately movable.

Abstract: A surgical device comprising a first jaw member, a second jaw member, a clamping member and a clamp apparatus is disclosed. The clamping member is slidably positioned to translate at least partially through the first jaw member. The clamping member engages the first jaw member and the second jaw member, and has a knife blade for cutting tissue. A flange of the clamping member is configured to engage a cam surface to pivot the second jaw member with respect to the first jaw member from an open position toward an approximated position. The clamp apparatus is movable from a retracted position to an advanced position for preventing a gap between proximal portions of the first jaw member and the second jaw member from exceeding a predetermined distance. The clamping member and the clamp apparatus are separately movable.

Abstract: There is provided a lumen maintenance catheter used for vascular suture, in which an operator can stably grip the catheter to improve the operability, and the entire catheter is prevented from entering a blood vessel. The lumen maintenance catheter for vascular suture includes a shaft having flexibility and a bulging part bulging in a radial direction at a distal end of the shaft, wherein the shaft includes a small diameter part on a distal end side, and a large diameter part larger in diameter than the small diameter part, on a rear end side, the small diameter part and the large diameter part are connected by an inclined part that is inclined so that a diameter of the shaft increases toward the rear end side, and the rigidity of the shaft increases as the diameter increases.

Abstract: An apparatus includes a body, a shaft extending distally from the body, a motor, a stapling assembly disposed at a distal end of the shaft, and a timer circuit operatively coupled to the motor and the firing actuator. The body includes a firing actuator and the motor is configured to activate in response to a firing actuation of the firing actuator. The motor is further configured to deactivate after a first predetermined time period subsequent to the firing actuation. The stapling assembly is configured to selectively move from an open position to a closed position to clamp tissue and is operable to drive a plurality of staples into the clamped tissue in response to activation of the motor. The timer circuit is configured to activate a timer in response to the firing actuation. The timer is configured to run for a second predetermined time period. The timer circuit is configured to ensure deactivation of the motor upon expiration of the second predetermined time period.

Abstract: Devices, systems, and methods for reducing stress on a blood vessel are disclosed herein. A damping device (100) configured in accordance with embodiments of the present technology can include an anchoring member (104) coupled to a flexible, compliant damping member (102) including a generally tubular sidewall having an outer surface (115), an inner surface (113) defining a lumen configured to direct blood flow, a first end portion (106) and a second end portion (108), and a damping region (120) between the first and second end portions (106, 108). The inner and outer surfaces (113, 115) of the damping member (102) can be spaced apart by a distance that is greater at the damping region (120) than at either of the first or second end portions (106, 108).

Abstract: Disclosed are coating compositions, processes, and designs for endowing vascular devices with thromboresistant and endothelializing properties. Also disclosed are designs of vascular devices used as aneurysm treating devices for assisting in the delivery, packing, and maintenance of embolization coils within an aneurysm, particularly a neurovascular aneurysm.

Abstract: Closure devices and methods for ligating tissue, such as the left atrial appendage, generally, include an elongate body having a first lumen therethrough, a snare loop assembly, a vacuum tube, and an imaging device. The snare loop assembly may include a snare and a suture loop releasably coupled to the snare and may at least partially extend from a distal end of the elongate body. The vacuum tube may be slidably positioned within the first lumen to extend through the snare loop assembly. The imaging device may be disposed within the lumen of the vacuum tube.

Abstract: A hemorrhage control device for sealing a penetrating wound includes a tube having a connector engaged to a first end thereof. The connector can selectively engage a container so that the container is in fluidic communication with the tube. The container can selectively pressurize a fluid positioned therein so that the fluid is selectively dispensable through the tube. A shell is engaged to a second end of, and in fluidic communication with, the tube. The shell is selectively expandable from a compacted configuration wherein the shell is substantially circumferentially equivalent to the tube. The shell can be at least partially inserted into a penetrating wound in a mammal, such as a bullet wound. The shell then can be selectively expanded, as the fluid is dispensed from the container through the tube, so that the shell contacts a surface of the penetrating wound to control hemorrhaging.

Abstract: Soft embolic implants exhibiting secondary shapes are disclosed. Some of the embolic implants exhibit progressively increasing softness from the distal end to the proximal end of the coil. The embolic implants have a primary coil, an optional second coil, a shape wire, and a stretch resistant fiber disposed in the lumen of the primary coil. An optional distal support wire is also disclosed. The embolic implants include a proximal constraint assembly configured to be releaseably retained by a delivery device. Disposed near each end of some of the implants are elliptical hole washers through which the shape wire and the stretch resistant fiber are threaded. The embolic implants have a primary, linear configuration for delivery through an implant tool, and a secondary configuration after deployment from the implant tool. The secondary shape can be J-shaped, helical, spherical, complex, or a combination of shapes.

Abstract: A method of implanting an occlusive device in a perforator vessel may include introducing a needle through skin of a patient, and advancing the needle into a perforator vessel, the perforator vessel extending between a superficial vein and a deep vein. The method may further include distally advancing a delivery component from within the needle until a distal end of the delivery component extends into the deep vein and releasing a distal portion of the occlusive device into the deep vein. The needle may then be proximally withdrawn from the perforator vessel such that the device is exposed within the vessel, and the proximal portion of the device may be released into the superficial vein such that the device blocks flow through the vessel.

Abstract: The present invention relates to a medical instrument, and particularly relates to a hemostatic clip device. The device includes a clamping component and a holder component. The head portion of the sleeve is provided with open slots for clamping arms to move. The tail ends of the outer side edges of clamping arms each is provided with a recess. A hole, corresponding to the position of the recess of one clamping arm, is formed in the other one. The sleeve is connected with the sleeve holder through inner core. The head end of the double-wire supporting arm is connected with the holes, and the other end is connected with wire rope and passes through the sleeve, the inner core, the sleeve holder and a bourdon tube so as to be connected with an operation handle. The device has the advantages of simple structure, firm clamping, convenient use and the like.

Abstract: Provided is a release device for medical tissue clips, including an outer tube provided with a release member, a control wire, and at least one tissue clip; wherein the release member is connected to the distal end of the control wire; the at least one tissue clip is movably connected to the release member and the control wire; the tissue clip includes a clip base and a clip piece which is movably disposed inside the clip base; the tissue clip is in a locked state when the clip piece is retreated to the proximal end, and in an opened state when the clip piece moves forwards to the distal end; the clip base includes an elastic member which is in a compressed state when being located in the outer tube and in an opened state upon detachment from the outer tube to abut against an end of the outer tube.

Abstract: The present invention relates generally to first aid articles and more specifically tourniquets suitable for one handed application. One embodiment of the invention is directed to a tourniquet having a base defining first and second ends. A constricting band is attached to and extends from the first end of the base. A handle is engaged with the constricting band. The constricting band engages a self cinching buckle which includes polygonal frame member and a self cinching member engaged with the polygonal frame member. A hook member is attached to the first end of the base and is configured to engage the polygonal frame member.

Abstract: A method for correcting position of an osteotomy guide tool and an orthopedic operation system are disclosed. A trackable element mounted on the osteotomy guide tool or on the robotic arm tracks the position of the osteotomy guide tool and generates position information of the trackable element. According to the current position and the desired position of the trackable element, a robotic arm drives the osteotomy guide tool and the trackable element to move, until the trackable element is moved to the desired position. This method does not need to consider the absolute position accuracy of the robotic arm, and does not rely on the experience of the surgeon. The tool has several guiding features, which can provide guides for osteotomy operations, so that the same osteotomy guide tool can perform multiple operations of osteotomy and punching, thus greatly reducing the operation time and improving the operation efficiency.

Abstract: A computer-assisted surgery system for guiding alterations to a bone, comprises a trackable member secured to the bone. The trackable member has a first inertial sensor unit producing orientation-based data. A positioning block is secured to the bone, and is adjustable once the positioning block is secured to the bone to be used to guide tools in altering the bone. The positioning block has a second inertial sensor unit producing orientation-based data. A processing system providing an orientation reference associating the bone to the trackable member comprises a signal interpreter for determining an orientation of the trackable member and of the positioning block. A parameter calculator calculates alteration parameters related to an actual orientation of the positioning block with respect to the bone.

Abstract: This invention relates to a surgical device for preparing the knee joint of a patient undergoing to partial knee replacement. The device is patient specific and has information about implant size, alignment and bone cut. This device consists of two parts, one is related to femoral template and the other one is related to tibial template. The femoral template positioned to a predefined location on the femur bone based on virtual planning of the surgery on specific software using 3D imaging. The femoral template allows to perform the posterior distal cut, drill and detect the location of the two holes relevant to the distal cut and implant pegs, while the tibial template allows the surgeon to make the tibial horizontal and vertical cuts; beside that, it has double slots which allows the surgeon to make extra bone removal if needed or when deciding to use larger size of polyethylene insert.

Abstract: An apparatus and kit for making holes of controlled depth and different diameters on chondral and osteochondral surfaces, comprises: a reamer member (2) having a cutting head (3) for removing tissue from said chondral and osteochondral surface (A), said member (2) being mobile approaching the chondral and osteochondral surface (A) for arranging the head (3) at said tissue; guide means (4) for guiding the reamer member (2) that can be firmly associated with the chondral or osteochondral surface (A), said reamer member (2) being slidable along said guide means (4); and mechanical means (5) for controlling the depth of the hole interposed between the reamer member (2) and the guide means (4) for defining an end stop of the reamer member (2) in the respective movement towards said chondral and osteochondral surface (A).

Abstract: The invention is directed to a surgical device which is externally used as aiming device that permits accurate placement of surgical wire to mend a supracondylar fracture. The device of the invention decreases operative time, risks of the re-dislocation through continuous manipulation, radiology exposure for both the patient and operation room staff, and to decreases anesthesia duration. It is also directed to surgical use of the device for repair of a supracondylar fracture and to methods for making it.

Abstract: A drill tap dilator comprises a dilator body having a central lumen extending therethrough, an elongate sleeve slidably received with the lumen, and a control knob coupled to the sleeve. The control knob is movable rotatably and axially relative to the dilator body. The sleeve includes docking teeth that are extendable from a retracted position within the body lumen to a deployed position outside the body lumen upon rotation of the control knob relative to the dilator body in one rotational direction. Adjustment of the length of drill tap dilator is allowed upon rotation of the control knob in an opposite rotational direction relative to the dilator body and manual axial movement of the control knob relative to the dilator body.

Abstract: A method and system for performing corrective surgery for pediatric or adult acquired flatfoot deformity (“AAFD”), namely, minimally invasive bone extra-articular reconstruction. The method and system comprises attaching a cutting guide to the bone to be operated wherein the cutting guide comprises two or more diverging K-wire channels and a slit configured to guide a burr used by a surgeon to perform osteotomy through the slit. Through the use of the cutting guide, the surgical procedure is simpler and reproducible. Patients will experience a quicker recovery, less pain, less operating room time, less narcotic use, and a better cosmetic result from smaller incisions. The present invention may also be applicable to intra-articular applications.

Abstract: An anchoring delivery system for use in an intracranial artery is provided including a tethering device having an elongated tether and an anchor coupled to a distal end of the tether. The anchor is deployable from a low profile configuration to a higher profile configuration to fix the distal end of the tether at an anchoring site in an anchoring vessel. The tethering device is configured to be used with a guide-sheath having a lumen configured to receive the tether. Related devices, systems, and methods are also described.

Abstract: Described are methods, systems, devices for facilitation of intraluminal medical procedures within the neurovasculature. A catheter advancement device includes a flexible elongate body having a proximal end, a distal end, and a single lumen extending therebetween. The flexible elongate body has a proximal segment, an intermediate segment, and a tip segment. The proximal segment includes a hypotube coated with a polymer. The intermediate segment includes an unreinforced polymer having a durometer of no more than 72D. The tip segment is formed of a polymer different from the intermediate segment and has a durometer of no more than about 35D and a length of at least 5 cm. The tip segment has a tapered portion that tapers distally from a first outer diameter to a second outer diameter over a length of between 1 and 3 cm.

Abstract: The invention involves forceps having rounded grasping tips. The rounded tips are configured to avoid puncturing an amniotic membrane during insertion over an ocular surface for the treatment of dry eye disease and inflammation of the eyes and to avoid injuring the conjunctiva during removal of an amniotic membrane from the ocular surface. The forceps have grasping tips at its distal end, wherein one of the grasping tips has a notch on its inside surface. The dimensions of the notch are configured to permit an eye doctor to securely and safely grasp a lip of an amniotic membrane insert for better insertion and removal from an ocular surface.

Abstract: A medical assistive device for quick positioning which can be combined with surgical reduction forceps rapidly, free from angle limitation, operated more conveniently. It comprises a base, the top surface thereof can hold the patient's wrist region; a socket holder located under the bottom surface of the base, provided with a round cavity-like hole slot; multiple support columns vertically located on the bottom surface of the base, surrounding the socket holder, forming connected passages under the base; a universal joint, embedded in the hole slot of socket holder, flexibly diverted. Thereby, the lower forceps body of surgical reduction forceps can reach the lower part of socket holder at any angle under the base, so that the lower forceps body is combined with the universal joint quickly, the combination is rapid, and the lower forceps body can rotate flexibly.

Abstract: An apparatus for disrupting tissue in the intervertebral disc space that includes a barrier member having a first configuration for insertion into the disc space and a second configuration when deployed within the disc space. The second configuration of the barrier member is adapted to at least partially define a perimeter of a working region within the disc space. The apparatus also includes a tissue disruption tool configured for insertion into the working region.

Abstract: A surgical cutting and fastening instrument is disclosed. According to various embodiments, the instrument includes an end effector comprising an elongate channel, a clamping member pivotably connected to the channel, and a moveable cutting instrument for traversing the channel to cut an object clamped in the end effector by the clamping member when the clamping member is in a clamped position. The instrument may also comprise a main drive shaft assembly for actuating the cutting instrument in the end effector, a gear drive train connected to the main drive shaft assembly, and a motor for actuating the gear drive train. The instrument may also includes a closure trigger and a firing trigger, separate from the closure trigger, for actuating the motor when the firing trigger is retracted. Also, the instrument may comprise a mechanical closure system connected to the closure trigger and to the clamping member for causing the clamping member to pivot to the clamped position when the closure trigger is retracted.

Abstract: An endoscopic surgical blade is disclosed. The blade is of a hook design, having an upper cutting surface located on the trailing edge of an arm and a lower cutting surface on the upper edge of the main body of the blade. The blade is part of an endoscopic knife assembly which also contains a knife tube and alignment ring. The endoscopic knife assembly is for use in endoscopic surgery by insertion of the assembly through a slotted cannula. The knife tube is hollow and allows the insertion of an endoscope for viewing of the surgical procedure. A method for a performing an operative procedure on a target tissue in a subject using an endoscopic knife assembly having a hook blade is also described.

Abstract: This document describes rotational atherectomy devices and systems for removing or reducing stenotic lesions in blood vessels by rotating an abrasive element within the vessel to partially or completely remove the stenotic lesion material.

Abstract: A catheter system (110) for removal of occlusive material in a body lumen. The catheter system (110) includes a catheter body (10), extending between a distal end (20) and a proximal end (22) and having a proximal portion (29) and a distal portion (28). The catheter body (10) includes a filtration section (30A) having filter media (32) configured to permit blood to pass through the lumen of the catheter body (10) and inhibiting occlusive material from passing out of the catheter body (10). The catheter system (110) also includes a control handle (120) coupled to the proximal portion (29) of the catheter body (10) and a cutter assembly (12) having a drive mechanism (40) operatively coupled to the control handle (120). The cutter assembly (12) includes a drive mechanism (40) and a conveyor (44) coupled to the drive mechanism (40) and rotatable with the drive mechanism (40) to convey occlusive material proximally within the catheter body (10) and through the filtration section (30A).

Abstract: An actuated telescoping system for navigation within a vascular lumen and thrombectomy of a thrombus. The system includes a tubular catheter member having an open distal end defining a catheter lumen, a vacuum source, a rotational drive system, a flexible shaft having a channel coupled to the rotational drive system for rotational movement in response thereto, and an optional guidewire selectively inserted at least partially within the flexible shaft. The flexible shaft is at least partially disposed within the tubular catheter member configured for uncoupled rotational and translational motion therein and to optionally define a corkscrew motion in response to rotational driving force by the drive system that results in formation of hydrodynamic vortices within the catheter lumen.

Abstract: An atherectomy catheter for use in a vessel includes an elongate catheter body and an annular cutter. The elongate catheter body includes a fixed jog section with a pre-set curvature and a flexible section that has a greater flexibility than a remainder of the elongate catheter body. The fixed jog section and flexible section are formed of a frame including a plurality of circumferential slits therein. Also described herein is an atherectomy catheter for use in a vessel includes an elongate catheter body, an annular cutter, and an s-shaped curved portion in the elongate catheter body. The curved portion includes a frame having a longitudinal proximal spine and a longitudinal distal spine. The longitudinal proximal spine is positioned approximately 180 degrees away from the longitudinal distal spine.

Abstract: Various devices and methods are provided with respect to inserting multiple surgical instruments through a single surgical access device. A medical device including a flexible tissue retractor a releasable insert having multiple instrument openings, and a member such as a sleeve is disclosed. The insert can be in the form of an insert assembly including multiple components. The sleeve can support the insert with respect to the retractor such that the insert and sleeve can be removed together with the retractor remaining in the incision. A method of using the insert is also described.

Abstract: A flexible fastening band connector can comprises a recess to receive a distal end portion of a flexible fastening band and lumen to receive the proximal end portion of the flexible fastening band. The lumen guides the proximal end portion of the flexible fastening band toward a fastening mechanism. The flexible fastening band connector can comprise an opening to receive a spinal rod. In operation, the spinal rod is coupled to additional devices to secure the spinal rod to portions of one or more vertebra. In some embodiments, a method of performing an operation, e.g. a spinal operation, on a patient using the disclosed connector is provided.

Abstract: A coupling device includes a first coupling body configured to be coupled to a first bone anchor, a second coupling body configured to be coupled a second bone anchor, and a connection device comprising a first connection member connectable to the first coupling body, a second connection member connectable to the second coupling body, and a length adjustment member positionable between and insertable at least partially into each of the first and second connection members. The first and second connection members are movable relative to the length adjustment member. The length adjustment member can be actuated in a first direction to increase a distance between the first connection member and the second connection member, and in a second direction different from the first direction to decrease the distance between the first connection member and the second connection member.

Abstract: A dynamic longitudinal connecting member assembly includes an anchor member having an integral or otherwise fixed elongate core of circular or non-circular cross-section. The core is pre-tensioned and extends through at least one elastic spacer and at least one outer sleeve. The anchor member and the outer sleeve each attach to at least one bone anchor. In operation, the core is held in tension by the spacer.