Abstract: An implantable medical device includes a support structure which is twistable in a longitudinal direction of the device. A sleeve of filter or occluding material is attached to the ends of the structure. The structure in practice twists on itself in the longitudinal direction, causing the sleeve to twist on itself and as a result to close the lumen through the sleeve. The device provides reliable closure and as a result occlusion of a vessel. It is also able to be delivered over a guide wire. In another embodiment, the support structure includes a wire which coils around the sleeve to constrict the sleeve and as a result to close a lumen of the sleeve.

Abstract: A surgical instrument includes a handle assembly, an elongate body, a tool assembly, and an electrical energy source. The handle assembly includes an actuation knob. The elongate body extends distally from the handle assembly and defines a longitudinal axis. In particular, tool assembly is operatively coupled to the handle assembly and extends from a distal end of the elongate body. The tool assembly includes first and second jaw members each including an electrically conductive cutting element. The cutting elements are operatively coupled to the actuation knob. In particular, the cutting elements are movable between a first position in which the cutting elements are disposed within the respective jaw members and a second position in which the cutting elements extend out of the respective jaw members and are in general vertical registration with each other such that electrical energy can be transferred from the first jaw member to the second jaw member.

Abstract: A suturing device is disclosed. The suturing device includes an end effector assembly disposed on a distal end of the suturing device. The end effector assembly includes at least one guide tube housing at least one elongated member, a clamshell, and a probe configured for disposal in a graft tubular tissue circumferentially offset from the clamshell. The probe includes at least one guide tube attached to a suture having a first end and a second end. The at least one elongated member is deployed to puncture graft tubular tissue and mate with the at least one aperture of the probe such that extraction of the at least one elongated member simultaneously draws out the suture through the punctured graft tubular tissue.

Abstract: A suture-needle holder includes: a sheath part; a grasping portion; an operation wire; and an operation part body formed to extend along a longitudinal axis, and connected such that the sheath part is movable in a direction aligned with the longitudinal axis and rotatable around the longitudinal axis. A first groove part having a distal end and a proximal end and extending along the longitudinal axis, and a second groove part having one end connected to the proximal end of the first groove part and the other end at a position separated from the one end in the direction aligned with the longitudinal axis and in a circumferential direction of the longitudinal axis, and extending from the one end to the other end are formed in the operation part body.

Abstract: Systems and methods are disclosed for delivering a stent to a lumen internal to a body of a patient and for sheathing a stent just prior to an insertion procedure. One embodiment comprises a delivery device having a partially sheathed configuration, a fully sheathed delivery configuration, and a deployed configuration. A panchor (combination pusher and anchor) is configured to engage and limit proximal and distal movement of the implantable device. An outer sheath surrounds a distal portion of an inner member and retains the implantable device near the distal end. The outer sheath is slidably moveable relative to the inner member to deploy the implantable device. Proximal movement of a trigger results in movement of the outer sheath to deploy the implantable device. A sheathing mechanism is configured to crimp and fully sheathe the implantable device prior to a deployment procedure.

Abstract: A tissue separation device includes: a sheath; a tube having a deformation part; a restriction member; and an inner structure. The tissue separation device is used in an assembled state where the tube is movably inserted in the sheath, the restriction member is inserted in the tube, and the inner structure is movably inserted in the restriction member. The inner structure includes: wires and which are expandable and contractible; an operation unit which operates expansion of the wires; a tubular body; and a traction shaft. The wires are expanded by being curved so as to protrude in opposite directions. When dissecting a biological tissue, the wires in an expanded state are moved within the tube in relation to the tube, without moving the tube relative to the living body.

Abstract: An endoscope treatment tool includes: a clip unit having a clip main body which includes first and second arm portions, a pressing tube which is formed in a tube shape, a locking portion which protrudes from an inner circumferential surface of a proximal end of the pressing tube, and a locked portion which protrudes from the clip main body; a linear member connected to the clip unit; a sheath in which the linear member is inserted; and a fracture mechanism connected to a proximal end of the linear member. The fracture mechanism includes a first support member connected to the linear member, a second support member disposed on a proximal end side of the first support member, and a fracturable member disposed between the first support member and the second support member so as to connect the first support member and the second support member.

Abstract: A valve holder is connectable to a prosthetic valve including a stent having a plurality of commissure posts. The valve includes a base, a plurality of legs extending from the base, and one of several mechanisms for deflecting the plurality of commissure posts radially inward so as to temporarily decrease the overall size of the prosthetic valve.

Abstract: A suture passing device includes a notchless tubular needle having a preformed curved shape. One or more cleats are disposed within the needle to help secure suture engaged by the sharp distal tip of the needle and to prevent further bifurcation of the suture. The deformable needle is housed in a channel of a lower jaw having a curved guidepath that approximates the curved geometry of the preformed needle, thereby facilitating the consistent return of the needle to its preformed shape each time the needle exits the channel. A dual needle suture passing device is also provided having a second notchless needle to enable a mattress stitch. Methods of loading a suture onto a notchless needle in a suture passer are also provided.

Abstract: Compressive plates of the placental insertion site for use in cases of placenta previa includes: an axle plate including a primary plate which is fixed, a threaded bar that has machined two plates and a diameter reduction section, a secondary plate having a hole with a diameter and a shape that allows the introduction of the bar, a punch with conical tip, a nut and a locknut, and a protective cover. The punch pierces the front and back walls of the uterus corresponding to the placental insertion site. Then, the secondary plate is introduced that approaches to the primary plate until obtaining enough pressure to stop the bleeding, the nut and locknut are placed, and, finally, the protective cover is screwed.

Abstract: A subintimal recanalization catheter system for recanalizing a blood vessel. The system includes a support catheter and a balloon catheter configured to extend through the support catheter. The support catheter includes a tubular portion and an extension segment extending distal of the distal opening of the tubular portion. The balloon catheter, having a balloon secured to a distal portion thereof, is positionable through the tubular portion of the support catheter to position the balloon alongside the extension segment. The system is configured to be advanced into a subintimal space between a first tissue layer and a second tissue layer of a blood vessel wall where the balloon may be inflated against the extension segment to cause a distal portion of the catheter shaft of the balloon catheter to deflect toward the vessel lumen within the subintimal space to facilitate reentry into the vessel lumen.

Abstract: Devices and methods for treating or repairing a heart are disclosed. The device includes at least one radially expandable tissue-engaging element, an elongate member (e.g., suture) coupled to the expandable element, and a locking mechanism (e.g., locking clip, suture knot). The expandable element may be anchored to heart tissue within the heart, such as in the left ventricle, with the elongate member extending from the expandable element and across a heart chamber to a second location such as the heart apex where the elongate member is held by the locking mechanism.

Abstract: The invention relates generally to embolic agents and embolic delivery systems more specifically it relates to a device and method for filling of aneurysm or body cavity. In various embodiments, segmented and monolithic embolic agents provide the operator with the ability to select and detach the length of embolic agent, either extracorporeally or intracorporeally as desired by the operator, for implantation into the aneurysm or body cavity. Linking elements and detachment elements may be utilized by the operator to connect and detach variable lengths of embolic agents either extracorporeally or intracorporeally utilizing electrolytic, chemical, and mechanical detachment mechanisms. Embolic delivery systems are disclosed providing for constant and steady propulsion of the embolic agent.

Abstract: Apparatuses and methods for controlling a medical device delivery assembly are provided. The apparatus can comprise a first engagement device and a coupling mechanism. The first engagement device can be used to engage a first component. The coupling mechanism can have a port and at least one wing. The at least one wing can be disposed adjacent to the port and be configured to facilitate interconnection of the first engagement device with the coupling mechanism.

Abstract: An apparatus for application of surgical clips to body tissue is provided and includes a handle assembly; a shaft assembly including a housing extending distally from the handle assembly and defining a longitudinal axis; a plurality of surgical clips disposed within the shaft assembly; a jaw mounted adjacent a distal end portion of the shaft assembly, the jaw being movable between an open spaced-apart condition and a closed approximated condition; and a pusher bar reciprocally disposed within the housing of the shaft assembly and being detachably connectable to the housing of the shaft assembly, the pusher bar being configured to load a distal-most surgical clip into the jaws during distal movement and remain connected to the housing of the shaft assembly and in a distally advanced position during an approximation of the jaws.

Abstract: A removable sleeve extends around an expandable stent graft to constrain the expandable stent graft toward a collapsed configuration. The sleeve is held together by a coupling member to constrain the expandable device toward the collapsed configuration for endoluminal delivery to a vascular treatment site. The sleeve is openable by displacing the coupling member away from the sleeve to allow outward expansion of the expandable device toward an expanded configuration. The sleeve is separate from the expandable device so as to be removable from the treatment site after deployment of the expandable device.

Abstract: A subintimal recanalization catheter, including an elongate shaft including a first tubular member and a penetration member slidably disposed in a lumen of the first tubular member. The penetration member includes a distal tip positioned proximal of a distal nose of the first tubular member. The distal nose of the first tubular member includes a ramp and a guide wire lumen extending through the distal nose of the first tubular member. Longitudinal movement of the penetration member relative to the first tubular member causes the penetration member to contact the ramp to direct the distal tip of the penetration member away from the first tubular member.

Abstract: A tunneling tool for implanting a medical device into body tissue is described. The tunneling tool comprises a first leg and a second leg. An intermediate portion of the second leg is shaped to nest a medical device therein. A hub connects the first and second distal leg ends together. A sheath providing a lumen extends from the hub to an open end distal of the first and second legs. The first and second legs are manipulatable to separate the hub and the sheath into two portions, a first split portion connected to the first leg and a second split portion connected to the second leg. When a medical device is nested in the tunneling tool, breaking the tunneling tool apart enables the first and second split portions to be removed from body tissue, leaving the implanted medical device behind.

Abstract: A surgical instrument includes a handle assembly, an elongate body, a tool assembly, and an electrical energy source. The handle assembly includes an actuation knob. The elongate body extends distally from the handle assembly and defines a longitudinal axis. In particular, tool assembly is operatively coupled to the handle assembly and extends from a distal end of the elongate body. The tool assembly includes first and second jaw members each including an electrically conductive cutting element. The cutting elements are operatively coupled to the actuation knob. In particular, the cutting elements are movable between a first position in which the cutting elements are disposed within the respective jaw members and a second position in which the cutting elements extend out of the respective jaw members and are in general vertical registration with each other such that electrical energy can be transferred from the first jaw member to the second jaw member.

Abstract: A delivery device for delivering material into a catheter through a catheter port includes a cannula having a generally tubular shape and a distal end and a stability collet having a distal attachment portion configured to attach the stability collet to a catheter port. The stability collet has a longitudinal channel through which the cannula extends. The longitudinal channel is dimensioned to allow a longitudinal movement of the cannula in the longitudinal channel. The delivery device further includes an elastic member acting between the cannula and the stability collet. The elastic member biases the cannula distally relative to the stability collet. Thus, when the stability collet is attached to the catheter port, the cannula is urged toward the catheter port, thus reducing a risk of improper alignment between the cannula and the catheter port.