Abstract: An illustrative example surgical method includes establishing a tunnel in a bone. At least a portion of the suture is passed through the tunnel. The suture has two ends and first and second loops between the two ends. The first loop includes a button on the suture. The second loop is on one side of the tunnel and the button is on the other side of the tunnel after the portion of the suture has been passed through the tunnel. At least some of the second loop of the suture is passed through soft tissue. Manipulating the second loop over the button positions a portion of the soft tissue between the second loop of the suture and the bone. Adjusting a length of the second loop urges the portion of the soft tissue against the bone where the portion of the soft tissue is held by the suture without tying any knots in the suture.

Abstract: A vascular filter system comprises a vascular filter (1), a clamp device (50), and a delivery catheter (51). The filter (1) comprises filter elements (6). When used without the clamp device (50), the filter elements (6) move from a closed state to an open state upon elapse of a predetermined period of time. In the closed state the filter elements (6) capture thrombus passing through the inferior vena cava (2). The delivery catheter (51) is employed to deliver the clamp device (50) to the filter (1) after the filter (1) has been deployed in the inferior vena cava (2). The clamp device (50) engages with the filter elements (6) of the filter (1) to clamp the filter (1) in the closed state beyond elapse of the predetermined period of time. Because of the presence of the clamp device (50), the filter elements (6) are no longer free to move from the closed state to the open state upon elapse of the predetermined period of time.

Abstract: The guidewire advancing device and method according to the present invention is used with a tubular catheter body configured to receive a hollow needle for receiving the guidewire. The guidewire advancing device includes the guidewire, guidewire housing, and means for advancing and retracting the guidewire. The means for advancing the guidewire includes a spool assembly or a slide tab and may also include a rack and pinion assembly for translation of forces to advance the guidewire.

Abstract: A system for retrieving an implanted medical device includes an outer tubular member and a contractible super-elastic net, which may be joined to an elongate shaft that extends in sliding engagement within the outer tubular member. When the net expands from a contracted condition the net defines a longitudinally extending tubular cavity. An open end of the cavity is sized to receive passage of a housing of the device therethrough; and the net, with the device housing contained therein, forms an interference fit within an inner diameter of the outer tubular member. But, an outer diameter of the net, in a fully expanded condition, is larger than the inner diameter.

Abstract: A catheter compiling a housing portion defining an interior cavity and the housing portion comprising a housing member having an interior space dimensioned for housing an indwelling medical device. The elongated member comprises a lumen extending at least from an exit port to a distal port, the housing member is disposed within the lumen, and the lumen is dimensioned in the housing portion to receive a guidewire outside of the interior space of the housing member. A medical device for filtering emboli from blood flowing in a blood vessel of patient comprising an elongate support member and an elongate side branch member connected to the elongate support member. The filter element is attached to the elongate side branch member by a proximal filter element slider, and the elongate side branch member is adapted to maintain the filter element centered in the vessel.

Abstract: A tissue pad is disclosed including a first component and a second component. The first component includes a first material and a first tissue engaging surface and the second component includes a second material and a second tissue engaging surface. The first component has proximal and distal ends and the second component has proximal and distal ends. The first and second components are separable. At least a portion of a distal end of the first tissue engaging surface is positioned distal relative to the second tissue engaging surface. The first material is different from the second material. The first material has a greater lubricity than the second material. The second material has a greater resistance to heat than the first material.

Abstract: A medical retrieval tool including a sheath; and a basket device connected to the sheath. The basket device includes a shaft and a basket located at a distal end of the shaft. The shaft is movably located in the sheath. The basket includes a first basket cage section and a second basket cage section. The first basket cage section is located in front of the second basket cage section. The basket is configured to be extended from a distal end of the sheath in a plurality of deployment modes including a first deployment mode where the first basket cage section is deployed in a first fully expanded shape and the second basket cage section is located in the sheath; and a second deployment mode where both the first basket cage section and the second basket cage section are deployed out of the distal end of the sheath.

Abstract: A prosthetic valve is advanced to a heart of a subject while the prosthetic valve is in a compressed state thereof, the prosthetic valve including a plurality of snares coupled to a tubular valve body. The prosthetic valve is positioned within the heart such that the plurality of snares is disposed upstream of the leaflets, and the plurality of snares is expanded upstream of the leaflets. Subsequently the prosthetic valve is moved in a downstream direction such that the plurality of snares is disposed downstream of the leaflets. Subsequently, the prosthetic valve is secured at the native valve while the plurality of snares remains disposed downstream of the leaflets.

Abstract: Tissue fasteners carried on a tissue piercing deployment wire fasten tissue layers of a mammalian body together include a first member, a second member, and a connecting member extending between the first and second members. One of the first and second members has a configuration alterable by a deployment wire to permit release of the fastener from the deployment wire after deployment and without causing excessive tissue trauma.

Abstract: A surgical device for suturing body lumen is described, as well as methods for suturing tissue employing the surgical device. The device can include a body having a shaft and a foot for insertion into an opening in a body lumen. The device can include tissue ports between configured to receive tissue surrounding the opening in the body lumen. The foot can include a suture secured to needle capture devices. The device can include needles that can be advanced through tissue and into the needle capture devices. The needle capture devices can then be withdrawn, thereby harvesting the suture, which can then be used to close the opening in the body lumen.

Abstract: An atherectomy device for removing deposits such as plaque from an interior of a vessel including an outer member and a rotatable shaft positioned for rotational movement within the outer member and fixed axially within the outer member. A tip is mounted to the distal region of the rotatable shaft and is positioned distally of the distal end of the outer member to create a gap between the proximal end of the rotatable tip and the distalmost edge of the outer member. The rotatable tip has a longitudinal axis mounted to the rotatable shaft for rotation about its longitudinal axis upon rotation of the shaft, the shaft including a guidewire lumen for receiving a guidewire to enable over the wire insertion of the device.

Abstract: A suture securing device includes a body connected to an arm by a hinge and is useable to secure a suture without requiring the tying of a knot. The body includes a bottom surface that contacts a patient's skin when in use, an eversion recess formed in the bottom surface, and a first gripping surface. The arm is connected to the body by the hinge and includes a second gripping surface that contacts at least a portion of the first gripping surface when the hinge is in the closed configuration. The device may also include an engagement structure configured to secure the arm to the body in the closed configuration.

Abstract: An anastomotic connector comprises a vessel anchor, a midgraft connector and graft material. The vessel anchor has a generally tubular main body including a distal end and a proximal end, the distal end defining a plurality of flanges integrally formed with the tubular main body and being movable from a first loaded position to a second expanded position. The midgraft connector operably couples the graft to the vessel anchor to form an anastomotic connector between an artery and a vein.

Abstract: A suture cinch, cinch applicator, and cinch loader for loading the cinch into the applicator are provided and permit re-use of the applicator with multiple cinches during an endoscopic procedure. The applicator can be loaded with a first cinch, apply the first cinch onto a portion of suture to fix the portion of suture relative to anatomical tissue, reloaded with a second cinch optionally using the loader, and subsequently used to apply the second cinch to fix another portion of suture to fix the other portion of suture relative to anatomical tissue. The cinch is a unitary tubular member through which the suture can be advanced when the cinch is loaded within the applicator. The cinch defines multiple ribs and a cutter in a wall thereof. Operation of the applicator deforms the ribs inward to retain the cinch on the suture and displaces the cutter to sever the suture.

Abstract: A system for implanting an implantable medical device (IMD) within a patient may include an IMD including an attachment member, and a delivery catheter including at least one tethering device having at least a portion positioned within a restrainer. The tethering device(s) is configured to removably tether to the attachment member of the IMD. The restrainer is configured to maintain the tethering device(s) in alignment along a delivery path of the delivery catheter.

Abstract: An atherectomy device for removing deposits such as plaque from an interior of a vessel including an outer member and a rotatable shaft positioned for rotational movement within the outer member. The outer member is fixed axially. A rotatable tip is mounted to the distal region of the rotatable shaft for rotation about its longitudinal axis upon rotation of the shaft. The rotatable shaft includes a guidewire lumen for receiving a guidewire to enable over the wire insertion of the device.

Abstract: The diameter of an annulus in a patient (e.g., the mitral valve annulus) can be reduced using a tissue engaging member that is installed on the annulus and an actuator that is implanted into the patient's body. The tissue engaging member has anchors used to implant the tissue engaging member into the annulus, and a cinching loop runs through the tissue engaging member. The cinching loop terminates onto cinching wires. Preferably, tissue healing is used to enhance the bond between the tissue engaging member and the annulus. The actuator, which can be actuated from outside the patient's body, pulls the cinching wires in a proximal direction while holding the distal end of the cinching wires in close proximity to each other, so as to cause a reduction in the diameter of the cinching loop. This will cause a corresponding reduction in the diameter of the annulus.

Abstract: A system is disclosed for performing hair transplantation procedures. The system may include a robotic arm and a tool coupled to the robotic arm, the tool configured for hair harvesting, site making or hair implantation. The system further includes a touch screen user interface that supports touch gestures for efficiently creating and manipulating objects, such as reserved regions, that control the harvesting, site making, and/or implantation sites selected by the system. The user interface implements logic rules that use the context in which a touch gesture is performed to determine the type of operation intended. The touch interface substantially eliminates or reduces the need for a user to use a keyboard or mouse during the procedure.

Abstract: A system for removing a thrombus. The system includes an expandable device that maintains axially fixed engagement with the thrombus. The expandable device applies a first force to the thrombus according to surrounding vessel size. The expandable device applies a second force to the thrombus according to an increased vessel size to maintain axially fixed engagement.

Abstract: Devices, systems and methods are described herein a prosthesis for implantation within a lumen or body cavity and delivery systems for delivering the prosthesis to a location for implantation. A delivery system can include a plurality of components, including a flexible nose cone, multi-layer sheath, and pre-compressed shaft, which can be moveable relative to each other.