Abstract: An anastomosis device includes magnets coupled to a wire capable of changing shape from a straight wire into a coil when deployed within a body. The coil exerts compressive force upon layers of tissue caught between loops of the coil. The compressive force is enhanced by attractive forces between magnets coupled with adjacent loops of the coil and causes the coil to cut through the tissue layers, creating an anastomosis. One end of the wire is preferably provided with a connecting member, such as a screw or a nut, for connecting with a delivery device.

Abstract: A compression ring to grip and compress body structure such as diverticulum, hemorrhoids, and tissue adjacent a hole. A resilient ring-shaped body defines a compression channel, and one or more axially rigid elongated spikes extend from the body into the channel. The body defines a first axial segment surrounding the compression channel and a second axial segment surrounding the compression channel, with the spike being engaged only with the second axial segment. The first axial segment more tightly compresses the body structure than the second axial segment.

Abstract: A surgical assembly includes a first guidewire and a second guidewire, in which each of the first guidewire and the second guidewire are configured to be received by a bone block, a first suture loop, a second suture loop, a first locking component, and a second locking component, in which the first locking component is coupled to the first suture loop and the second locking component is coupled to the second suture loop. The locking component has a hole formed therethrough, in which the hole of the locking component is configured to receive the suture, and may be tethered to a suture by knots engaging a counterbore at opposed ends of a bore defined by the hole.

Abstract: A tissue-fastening tool indwelling device includes: a sheath; a needle tube having a needle tip and disposed to be retractable from a distal end of a lumen of the sheath; a tissue-fastening tool having a restoring force to a curved shape with distal and proximal end side regions and disposed inside the needle tube in a stretched state; and a stylet coupled to a proximal end portion of the tissue-fastening tool in the needle tube. The stylet has a first state in which the stylet is advanced straight with respect to the needle tube and the sheath until the entire distal end side region of the tissue-fastening tool protrudes from the needle tube, and a second state in which the stylet is advanced while being rotated until a proximal end of the proximal end side region of the tissue-fastening tool protrudes from the needle tube.

Abstract: Devices, systems and methods for retracting, lifting, compressing, supporting or repositioning tissues, organs, anatomical structures, grafts or other structures within the body of human or animal subjects for the purpose of treating a diseases or disorders and/or for cosmetic or reconstructive purposes and/or for research and development purposes or other purposes.

Abstract: A medical device including a first layer having an opening formed therein. A second layer is positioned with respect to the first layer to form a pocket therebetween. A support member is at least partially located in the pocket and reconfigurable for removal of the support member from the pocket via the opening. An affixation element located in the pocket between the support member and the second layer, and secured to the second layer. A method of implanting a medical device is also included.

Abstract: Suture anchors and associated methods are disclosed having suture locking features able to lock multiple suture ends extending from a body tissue, such as from a bone tunnel, with a single device.

Abstract: Implants for the treatment of pelvic support conditions and methods of implementing the same. The implants comprise relatively soft, flexible bodies and relatively strong arms extending in predetermined orientations therefrom. Methods and devices for placing the implants minimize trauma to the pelvic floor and provide well-anchored support to pelvic organs without interfering with sexual or other bodily functions.

Abstract: Absorbable polyester fibers, braids, and surgical meshes with prolonged strength retention have been developed. These devices are preferably derived from biocompatible copolymers or homopolymers of 4-hydroxybutyrate. These devices provide a wider range of in vivo strength retention properties than are currently available, and could offer additional benefits such as anti-adhesion properties, reduced risks of infection or other post-operative problems resulting from absorption and eventual elimination of the device, and competitive cost. The devices may also be particularly suitable for use in pediatric populations where their absorption should not hinder growth, and provide in all patient populations wound healing with long-term mechanical stability. The devices may additionally be combined with autologous, allogenic and/or xenogenic tissues to provide implants with improved mechanical, biological and handling properties.

Abstract: A system for implanting a repair device onto a native valve of a natural heart to repair the native valve of a patient during a non-open-heart procedure. The system includes a surgical delivery instrument and a valve repair device. The surgical delivery instrument has at least one lumen. The valve repair device is configured to be delivered through the lumen of the surgical delivery instrument and to be attached to a native valve of a patient. The valve repair device includes a pair of paddles and a pair of gripping members. The paddles are movable between an open position and a closed position, and the paddles are configured to flex upon being attached to the native valve of a patient. The paddles and the gripping members are configured to attach to the native valve of the patient.

Abstract: Techniques for mesh augmentation and prevention of incisional hernia, including systems and methods for affixing mesh to a fascial incision. A mesh strip can be integrated with one or more uni-directional fasteners. Each fastener can include an anchoring mechanism adapted for affixation to anterior abdominal wall fascia and a mating interface. An applicator can include tension arms adapted to interface with the mating interfaces of the fasteners to maintain a vertical tension of the mesh strip and a handle coupled with the tension arms adapted to spread the tension arms and thereby control a horizontal tension of the mesh strip. The mesh strip can be configured to be aligned over a fascial incision using the applicator and affixed under tension to anterior abdominal wall fascia by tissue penetration of the anchoring mechanisms of the one or more fasteners.

Abstract: A multilayer composite cloth with different flexibility and scalability can be used in wearing articles. The multilayer composite cloth has at least two surface-overlaid stretch cloths to present a multilayer composite structure. An elastic enhancement strip is bound between the two stretch cloths and corresponds to local area of the two stretch cloths, enabling the distribution area of the elastic enhancement strip to generate different elasticity. The elastic enhancement strip is hidden between the stretch cloths but does not appear on the surface of the composite co-structure cloth, thus enabling the composite co-structure cloth to present one cloth pattern with different elasticity and scalability. This cloth used in wearing articles will provide binding, support or bracing to muscles or joints maintain aesthetics of wearing articles and achieve the goals of protection, reducing injury probability, slimming and beauty.

Abstract: Absorbable polyester fibers, braids, and surgical meshes with prolonged strength retention have been developed. These devices are preferably derived from biocompatible copolymers or homopolymers of 4-hydroxybutyrate. These devices provide a wider range of in vivo strength retention properties than are currently available, and could offer additional benefits such as anti-adhesion properties, reduced risks of infection or other post-operative problems resulting from absorption and eventual elimination of the device, and competitive cost. The devices may also be particularly suitable for use in pediatric populations where their absorption should not hinder growth, and provide in all patient populations wound healing with long-term mechanical stability. The devices may additionally be combined with autologous, allogenic and/or xenogenic tissues to provide implants with improved mechanical, biological and handling properties.

Abstract: A delivery device and implantable prosthesis for repairing a soft tissue defect such as an abdominal wall hernia. The delivery device includes a support body that is nested between a first and second layer of the prosthesis. The support body includes a zone of weakness to facilitate collapse of the nested delivery device and prosthesis. A handle extends from the support body and may be used to position the prosthesis as well as to cause the support body to move to a reduced configuration for removal of the support body from the prosthesis.

Abstract: A thermoresponsive polyester comprising units derived from an amide functional diol compound having a first amide group having a nitrogen atom and a carbonyl group; a second amide group tethered directly or indirectly through an organic group at the carbonyl group of the first amide group; and two organic groups terminated with a hydroxyl group attached to the nitrogen atom of the first amide group. The thermoresponsive polyesters exhibit a lower critical solution temperature at which they undergo a thermally induced reversible hydrophobicity change. This hydrophobicity change may involve the formation of coacervates of the thermoresponsive polyesters which can then coalesce into a precipitated polymer rich phase.

Abstract: Various embodiments of a trocar or needle system for use in inserting and deploying pelvic implants are provided. The needle device can include a solid or hollow shaft portion with a non-circular cross-section. A grip element can be provided to slide along a length of the needle shaft to further facilitate handling.

Abstract: Absorbable composite medical devices such as surgical meshes and braided sutures, which display two or more absorption/biodegradation and breaking strength retention profiles and exhibit unique properties in different clinical settings, are made using combinations of at least two types of yarns having distinctly different physicochemical and biological properties and incorporate in the subject construct special designs to provide a range of unique properties as clinically useful implants.

Abstract: Thoracic/lumbar and cervical spinous process staples which staple/fuse adjacent spinous processes are disclosed. Thoracic/lumbar transverse process staples which staple/fuse adjacent transverse processes are also disclosed. Each embodiment has upper and lower claws connected by a ratchet spring mechanism, along with a multiplicity of bone fastener prongs attached to the upper and lower claws. Two sets of prongs on each staple claw are spaced by a distance approximately equal to the distance separating adjacent spinous or transverse processes so as to facilitate stapling/fusion of two adjacent processes. Also disclosed are staple prongs with multiple perforations which enable incorporation of bone fusion material thereby facilitating stapling/fusion of spinal elements.

Abstract: A tissue grasping tool includes: a longitudinal-axis member; a first member and second member; a manipulation member; a first wire-shaped member protruding from the first member and being formed a first loop; and a second wire-shaped member protruding from the second member and being formed a second loop; the first wire-shaped member and the second wire-shaped member extend in a direction which gradually approaches with each other as it goes toward the distal side from a proximal side of the first and second loops; in a state of which the first member and the second member come close with each other, the second wire-shaped member passes through an inside of the first loop; and a distance between distal end portions of the first and second loops is increased according to an operation in which the first member and the second member approach.

Abstract: A therapeutic delivery device comprises a layer of biodegradable material wound into a plurality of windings, the plurality of windings comprising an outermost winding defining an internal volume and winding pairs including a first winding pair and a second winding pair. A first therapeutic mass is incorporated in or on the layer the first winding pair and a second therapeutic mass is incorporated in or on the layer along the second winding pair. In one implementation, at least one volume of gas is captured within the internal volume and occupies at least 50% of the internal volume. In one implementation, the windings include perforations.

Abstract: Vasculature closure devices, and systems and methods for their use, are provided. In one or more embodiments, a vasculature closure device (200) includes an expandable support frame (210) deployable within a vessel (10), and a sealing membrane (205) at least partially supported by the support frame (210). Upon expanding the support frame (210) within the vessel (10), the device is configured to intraluminally position the sealing membrane (205) against a puncture site existing in a wall of the vessel. The sealing membrane includes an area of excess membrane (245) configured to facilitate coupling of the sealing membrane to the wall of the vessel.

Abstract: Systems, apparatus, and methods may be adapted for grafting tissue at a tissue site that may include an elongate housing and a plurality of elongate cutting members. The plurality of elongate cutting members may define a cutting surface at a distal end of the elongate housing. The cutting surface may be adapted to contract from a first diameter to a second diameter that is less than the first diameter. The contraction of the cutting surface from the first diameter to the second diameter may define a tapered profile between the first diameter and the second diameter suitable for obtaining a tapered graft.

Abstract: A mosaic implant conformable to a curved surface, comprising first and second implant sections coupled along a beam portion extending across a length of the implant, each of the implant sections having—a plurality of biocompatible mosaic plates, and—a plurality of wires which interconnect the plates with one another. The mosaic implant is configured to be deformable such that at least a portion of the mosaic implant is conformable to a curved surface, with the beam portion providing structural support which resists inward deformation of the curved portion of the implant. A kit for forming a mosaic implant is also provided, along with a method for correcting a bone defect in a patient.

Abstract: A method of treating urinary incontinence is disclosed. The method includes guiding a tip of an introducer tool through a length of a soft tissue anchor and out of an end of the soft tissue anchor. The method includes pushing the tip of the introducer tool and the soft tissue anchor into tissue on a side of a urethra, penetrating the tissue with the tip of the introducer tool, and delivering the soft tissue anchor into the tissue. The method includes removing the tip of the introducer tool from the soft tissue anchor and allowing a plurality of projections connected to the soft tissue anchor to expand thus anchoring the soft tissue anchor in the tissue.

Abstract: A spacer fabric mesh comprising: a spacer fabric comprising: a bottom fabric layer; a top fabric layer; and an intermediate layer comprising a plurality of interconnecting fibers which extend between, and connect, said bottom layer and said top layer, wherein said interconnecting fibers have sufficient resilience and stiffness to keep said bottom layer and said top layer separated when pressure is applied to at least one of said bottom layer and said top layer.

Abstract: A surgical clamp assembly 100 for use in keyhole surgery is disclosed. The assembly includes: a surgical clamp 10 for forming a clamping loop around a bodily lumen 8. The clamp includes: a strap 20, the strap including an elongate grippable portion 23; and a head 30 including a gripper 40, the gripper having an open mouth, the open mouth shaped to allow lateral entry of the strap into the gripper so as to form the clamping loop. The assembly further includes: a deployment tube 60 for deploying the clamp through a keyhole; and a manipulator 70 for manipulating the clamp through the deployment tube. The elongate body is biased to move from a constrained generally straight condition within the deployment tube to an unrestrained curled condition within a patient. A surgical clamp assembly, that includes a surgical clamp is also disclosed.

Abstract: A method for securing soft tissue to bone which does not require the surgeon to tie suture knots to secure the tissue to the bone. Suture is passed through the tissue at desired points. A cannulated plug or screw is pre-loaded onto the distal end of a driver provided with an eyelet implant at its distal end. Suture attached to the tissue is passed through the eyelet of the implant located at the distal end of the driver. The distal end of the driver together with the eyelet implant is inserted into the bone. Tension is applied to the suture to position the tissue at the desired location relative to the bone. The screw or plug is advanced into the pilot hole by turning the interference screw or tapping the plug until the cannulated screw or plug securely engages and locks in the eyelet implant, so that the cannulated plug or screw with the engaged eyelet implant is flush with the bone.

Abstract: A surgical implant (1) comprises a basic structure (2) having a first face (4) and a resorbable film (6) attached to the first face (4) of the basic structure (2). A plurality of solid protrusions (8) emerges from the film (6) in a direction away from the basic structure (2). The protrusions (8) comprise a shape defined by a respective body and a respective head, the body emerging from the film (6) and terminating in the head, and the head projecting laterally with respect to the body.

Abstract: Described herein is a bike including a frame member linking the front and rear wheel(s) made up of a first forward section or sections extending from the front wheel(s) and a second rear section or sections extending from the rear wheel(s). The section endings mate about a lockable connection assembly that is also in communication with a seat-post connected to the seat. The frame sections pivot about a connection assembly axis in a direction perpendicular to the bike frame and the seat-post is able to be moved independent of the frame sections. A key advantage of the above bike is the high range of height adjustability allowing the bike to be used by range of different sized users. Height adjustment is also very easy and may be done toolessly. Further, maintaining the seat in a desired riding alignment independent of frame movement is important otherwise the rider position will change relative to the handlebars leading in extreme cases to falls from the bike.

Abstract: This invention generally relates to a device and method for repairing biological tissue aperture. In certain embodiments, the invention provides a system for closing an aperture in a biological tissue that includes a handle, a shaft connected to the handle, and a deployment scaffold connected to the shaft, in which the scaffold is configured to releasably retain a surgical implant and the scaffold includes an open configuration and a closed configuration, the open configuration being substantially X-shaped.

Abstract: Systems and methods for modifying a heart valve annulus in a minimally invasive surgical procedure. A helical anchor is provided, having a memory set to a coiled shape or state. The helical anchor is further configured to self-revert from a substantially straight state to the coiled state. The helical anchor is loaded within a needle that constrains the helical anchor to the substantially straight state. The needle is delivered to the valve annulus and inserted into tissue of the annulus. The helical anchor is then deployed from the needle (e.g., the needle is retracted from over the helical anchor). Once deployed, the helical anchor self-transitions toward the coiled shape, cinching engaged tissue of the valve annulus.

Abstract: The present disclosure provides an endovascular device for treating a defect in the vascular wall such as aneurysm by deploying a self expandable barrier around the aneurysm neck to block the blood flow to the aneurysm and method for implementing the endovascular device. The endovascular device also allows for delivery of certain swellable materials and bioactive materials, such as thrombogenic compounds, to the aneurysm to accelerate occlusion and healing of the aneurysm.

Abstract: Closure systems, kits and methods for sealing a percutaneous puncture or other opening in a blood vessel wall, body cavity or biopsy tract are disclosed. A closure system can comprise an implant assembly, a delivery assembly, and an introducer sheath. The closure system can further comprise a valve bypass and a dilator. The implant assembly can include an inner member, a sealing membrane, and an outer member, each of which can be delivered by the delivery assembly. The inner member can be extended through the puncture or opening and positioned adjacent an inner tissue surface. The outer member can be positioned adjacent an outer tissue surface. The sealing membrane can have a distal end attached to the inner member, a proximal end including an opening configured to receive the outer member, and a mid-region therebetween.

Abstract: Tissue implants prepared for the repair of tissues, especially avascular tissues such as cartilage. One embodiment presents an electric potential capable of receiving and accumulating desirable factors or molecules from surrounding fluid when exposed to dynamic loading. In another embodiment the implant promotes tissue conduction by retarding, restricting and controlling cellular invasion through use of gradients until competent tissue forms. Further embodiments of the tissue implants may be formed into a multi-phasic device that provides deep tissue mechanical stimulus by conduction of mechanical and fluid forces experienced at the surface of the implant.

Abstract: A buckle useful for cortical fixation has a graft retention loop slidably affixed thereto for movement from a first position adjacent a first end of the buckle to a second position at about the midpoint of the buckle. The buckle, with a graft over the loop, is drawn up lengthwise through a bone tunnel through a tibia and then flipped sideways to rest against the surface of the bone with the loop and graft depending back into the tunnel. The sliding attachment of the loop permits flipping of the buckle minimizes the flipping distance, which is the excess amount of the loop which must be pulled free of the tunnel to allow the buckle to be flipped sideways.

Abstract: A gastric restraining device for treating excessive weight or obesity in mammals. The gastric restraining device includes an elastomeric sheet configured to be placed around a stomach of a mammal, an ablation device attached to the elastomeric sheet, the ablation device configured to emit energy toward an outer surface of the stomach when the elastomeric sheet is placed around the stomach, and an energy device coupled to the ablation device to generate the energy and to transfer the energy to the ablation device.

Abstract: A bone plate system is provided that permits rapid, secure stabilization of a plurality of bones, such as portions of a cut rib. The bone plate system includes a bone plate having anchor devices for securing the bone plate to, for example, cortical bone of the cut rib portions. The anchor devices have an open configuration that permits the anchor devices to be connected to the cortical bone of the cut rib portions and a clamping configuration that fixes the bone plate to the cortical bone of the cut portions. The bone plate connects the cut rib portions and stabilizes the cut rib portions against relative movement therebetween.

Abstract: An anchorage in tissue is produced by holding a vibrating element and a counter element against each other such that their contact faces are in contact with each other, wherein at least one of the contact faces includes a thermoplastic material which is liquefiable by mechanical vibration. While holding and then moving the two elements against each other, the vibrating element is vibrated and due to the vibration the thermoplastic material is liquefied between the contact faces, and due to the relative movement is made to flow from between the contact faces and to penetrate tissue located adjacent to outer edges of the contact faces. For liquefaction of the thermoplastic material and for displacing it from between the contact faces, no force needs to act on the tissue surface which is to be penetrated by the liquefied material.

Abstract: Two minimally invasive therapeutic procedures, particularly for patients with congestive heart failure, may be performed separately or together. One procedure involves providing a valved passageway through the patient's left ventricular wall at the apex of the patient's heart and advancing instruments through the valved passageway to connect the valve leaflets of the patient's heart valve, e.g. the mitral valve. The second procedure involves advancing a pacing lead and a pacing lead implanting device through a trocar in the patient's chest and implanting the pacing lead on an exposed epicardial region of the patient's heart wall. The pacing lead has a penetrating electrode which is secured within the heart wall. Improved devices for these procedures include a minimally invasive grasping device for heart leaflets, a leaflet connector with artificial cordae tendenae and a pacing lead implant instrument.

Abstract: The present invention generally relates to devices and methods for reversibly coupling an implant to a deployment device.

Abstract: Described are pelvic implants and methods of surgically placing pelvic implants, the implants optionally including the ability to engage a spreader tool for spreading the implant within the patient, also optionally including a stiffening frame (306), exemplary implants being capable of being used to treat pelvic floor disorders, for example by supporting of levator tissue.

Abstract: A device having one or more adjustable loops or coils associated with an implant body for use in soft tissue reconstructions is provided. One exemplary embodiment of a device includes a body and a suture filament, with the filament being used to form a self-locking sliding knot disposed on a top side of the body and a plurality of adjustable coils that are substantially disposed on the body's bottom side. Terminal ends of the filament located above the body's top side can be passed through an opening of a Lark's Head knot from opposite sides, thus forming a self-locking sliding knot, and then the terminal ends can be tensioned to adjust a circumference of the coils. Changing a coil's circumference changes a location of a ligament graft disposed on the coil. Other configurations of devices and systems, as well as methods for performing ACL repairs, are also provided.

Abstract: Prosthesis (1) comprising a patch (2) made of biocompatible material, said patch having a generally plane geometric shape that defines two opposite faces, a center, a length and a width of said patch, characterized in that said patch is provided, on one (2a) of its faces, with a single marking means (3) designed to indicate both the center (C) of the patch and also the longitudinal direction of said patch.

Abstract: A spinal fusion system may include an interbody fusion cage, a fixation plate, and an implanter. The interbody fusion cage may include a proximal region, a distal region opposite the proximal region, a superior region, an inferior region opposite the superior region, and an open volume between the proximal and distal regions. The superior and inferior regions are located between the proximal and distal regions and are configured such that, when the interbody fusion cage is implanted in the disc space, the superior region contacts the inferior end plate and the inferior region contacts the superior end plate. The fixation plate is receivable in the open volume of the interbody fusion cage and includes a superior blade and an inferior blade. At least one of the blades includes a first opening defined therein. The fixation plate is displaceable between a non-deployed state and a deployed state.

Abstract: A handle for surgical instruments that has a “wishbone” configuration. In one embodiment, the instrument is provided with a ratchet mechanism allows two operating handles to be locked in a predetermined position (for example, when the surgical instrument that is maneuvered is in use) or to move relative to each other when the ratchet is partially or fully released (for example, when the surgical instrument that is maneuvered is not in use). In another embodiment, the instrument is provided with a rotary gear mechanism.

Abstract: The present invention relates to closing an opening within a subcutaneous bodily vessel by using a spiral closure device to engage tissue around the opening. The spiral closure device is adapted to be threaded into the vessel wall surrounding the opening in the bodily vessel. A deployment mechanism may be used to rotate the spiral closure device. As the deployment mechanism is rotated the spiral closure device is rotated such that a tip of the spiral closure device engages the vessel wall around the opening in the bodily vessel. Continued rotation of the spiral closure device threads the closure device through the tissue around the opening. The closure device may have a tapered configuration in which the distal end is larger than the proximal end. As the distal end is threaded through the vessel wall, the narrowing closure device pulls the vessel wall tissue together, thereby effectively closing the opening.

Abstract: To increase the resistance to liquid and substance flow through a lumen of a tubular organ, a cuff comprising a flexible, mesh base member is appended to an exterior wall of the tubular organ such that it only partially surrounds the tubular organ. Ultimately, tissue ingrowth through the mesh base member integrates the cuff into the wall of the tubular organ. When the cuff is applied to the urethra of an incontinent patient, the increased resistance to flow renders the patient continent while still allowing normal voiding. The base member may also support an optional expandable component, e.g., a balloon-like element that can be selectively inflated and/or deflated to restrict the lumen of the tubular organ by a desired degree.

Abstract: Implant for supporting bodily conduits, such as blood vessels or/and grafted vessels, inside a subject. In exemplary embodiments, the implant includes a support fixedly displaceable and plastically stretchable to points along longitudinal axis of the support, when subjected to a stretching force, thereby forming a new shape, the support substantially maintains the new shape upon removal of the stretching force. The support, when forming the new shape, is plastically reversely compressible in a direction along the support longitudinal axis, when subjected to axially compressive force. Support may include a radially elastic portion configured to regain fixedly deformed diameter upon removal of radially compressive force applied thereto. Support is configurable as an intraluminal support for intraluminal deployment and setting in a conduit segment, or, as an external support for enveloping a conduit segment, so as to change route or/and shape of the conduit segment.

Abstract: A method of treating pelvic organ prolapse in a female patient by accessing a prolapsed organ trans-vaginally through a vagina is disclosed. The method includes making an incision through a wall of a vagina of the female patient, and providing an implant with a mesh having a mass density of 50 g/m2 or less. The method additionally includes radially confining the implant with a tool, and inserting a portion of the tool and the implant through the incision formed in the wall of the vagina. The method includes releasing the implant from the tool in an area of the prolapsed organ in supporting the vagina of the female patient.

Abstract: Among other things, there is disclosed devices for closing an internal opening, e.g. a hole in a blood vessel, that includes a shape memory function. Particular substances have been found to provide advantages in use, and in particular forms of closure structures.