Abstract: This material comprises an annuloplasty member able to be introduced using a catheter through minimally invasive vascular access, then to be delivered by said catheter and fixed to the valve annulus. According to the invention, it includes at least one catheter comprising at least one guide member able to be deployed from said catheter such that it extends along one portion of the valve annulus of the valve, in the immediate proximity of said valve annulus, and an implant having a helical shape engaged on said guide member, connected, with separation possibility, to actuation means making it possible to cause this implant to move forward while driving it in rotation around its axis; the implant can thus be deployed from the catheter while being simultaneously moved forward and driven in rotation along its axis.

Abstract: The present disclosure relates to an arrangement, a loop-shaped support, a prosthetic heart valve and a method of repairing or replacing a native heart valve. With the method or the arrangement, leakage or regurgitation between a prosthetic heart valve and the surrounding valve tissue is prevented. In one embodiment, an arrangement for replacement or repair of a native heart valve is provided, which comprises a loop-shaped support 41 and a prosthetic heart valve 70 and wherein an outer segment 32 of the loop-shaped support 41 is positionable towards surrounding valve tissue of a native heart valve and wherein an outer surface 74 of the prosthetic heart valve 70 is positionable towards an inner segment 34 of the loop-shaped support 41 so as to prevent paravalvular leakage or regurgitation between the prosthetic heart valve 70 and the surrounding valve tissue of the native heart valve.

Abstract: A surgical filament snare assembly including an anchor capable of being fixated in bone and having a filament engagement feature. A first filament has a noose on a first portion of at least a first limb and has a second portion connected to the filament engagement feature of the anchor. Preferably, at least one free filament limb, which in some embodiments is a length of the first filament and in other embodiments is a second filament, is capable of being passed through tissue to be repaired and has at least one end passable through the noose to enable incremental tensioning of the tissue after the anchor is fixated in bone. The noose strangulates the free filament limb when tension is applied to at least one of the free filament limb and the noose.

Abstract: A surgical bur is disclosed having cutting and trailing edges and associated flutes and lands. Each flute includes a cutting edge. Each of the trailing edges relatives in a selected dimension to a preceding cutting edge.

Abstract: Various systems, devices and methods associated with the placement of a dock or anchor (72) for a prosthetic mitral valve (120). The anchor (72) may take the form of a helical anchor having multiple coils (104, 108) and/or a stent-like structure. Various methods include different levels of minimal invasive procedures for delivering the prosthetic valve anchor (72) and prosthetic valve (120), as well as tissue anchors for plication or other purposes to the mitral valve position in the heart (14).

Abstract: An end effector for use and connection to a robot arm of a robotic surgical system, wherein the end effector is controlled and/or articulated by at least one cable extending from a respective motor of a control device of the robot surgical system, is provided. The end effector includes at least one gear train that transmits forces from the at least one motor of the control device to at least one of the proximal bracket of the wrist assembly, the distal bracket of the wrist assembly and the jaw assembly. The gear train enables at least one of a pivoting of the distal hub assembly relative to the proximal hub; a rotation of the distal bracket relative to the proximal bracket; and an opening/closing of the jaw assembly.

Abstract: A percutaneous heart valve prosthesis (1) has a valve body (2) with a passage (9) extending between the first and second ends (7, 8) of the valve body (2). The valve body (2) is collapsible about a longitudinal axis (10) of the passage (9) for delivery of the valve body (2) via a catheter (18). One or more flexible valve leaflets (3, 4) are secured to the valve body (2) and extend across the passage (9) for blocking bloodflow in one direction through the passage (9). An anchor device (5), which is also collapsible for delivery via catheter (18), is secured to the valve body (2) by way of an anchor line (6). A failed or failing mitral heart valve (101) is treated by percutaneously locating the valve body (2) in the mitral valve orifice (102) with the anchor device (5) located in the right atrium (107) and engaging the inter-atrial septum (103), such that the taught anchor line (6) acts to secure the valve body (2) within the mitral valve orifice (102).

Abstract: A force-directional nasal surgery dilatation device for use in a medical procedure such as sinuplasty, correction of deviated septum, and expansion of sinus cavities and nasal passages. An inflatable balloon is affixed to the distal end of a shaft for supporting and guiding the balloon into position for a nasal surgery procedure involving a patient. The shaft includes an inflation passageway associated for introducing an inflation medium into the balloon. The device further includes a force distribution member affixed to the inflatable balloon that provides a relatively rigid surface for applying distributed force against a tissue in the patient's nasal cavity upon inflation of the balloon. The force distribution member can include a pair of generally planar articulated adjacent surfaces attached along a hinge line between the surfaces.

Abstract: The present embodiments provide prosthesis deployment systems. In one embodiment, a sleeve has proximal and distal regions and a lumen extending therebetween, and further comprising a first exit aperture, a first entrance aperture, and a second exit aperture. A trigger wire is disposed at least partially within the lumen of the sleeve. A prosthesis has a delivery state and an expanded state, and further has first and second regions. In the delivery state, the trigger wire extends out of the lumen through the first exit aperture of the sleeve, restrains the first region of the prosthesis, reenters the lumen through the first entrance aperture of the sleeve, extends out of the lumen through the second exit aperture of the sleeve, and restrains the second region of the prosthesis.

Abstract: A hydraulically-driven Intra-Ocular Lens (IOL) insertion tool includes a body, a chamber within the body, a first fluid port providing fluid communication into the chamber, a piston positioned within the chamber and arranged to move within the chamber in response to the introduction or removal of fluid from the chamber, and an elongated member. The elongated member includes a distal end comprising an intra-ocular lens interface and a proximal end connected to the piston such that movement of the piston within the chamber causes corresponding movement of the elongated member.

Abstract: An actuation method for a surgical tool and the tool itself, which includes a proximal coupling portion from which two hydraulically actuatable, pivotably connected members extend. Each of the branches, at least at their distal ends, have an active portion and form in the coupling portion a boundary for at least part of a fluid-tight, fluid-fillable cavity. A pivot position of the members and a volume of the fluid in the cavity are operatively coupled with one another. An actuation method for a micro-surgical tool and the micro-surgical tool, which includes a proximal handle with an actuation device and a distally disposed inventive hydraulically actuatable surgical tool, which is connected by a shaft with the handle and can be actuated by the actuation device.

Abstract: A system for implanting an anchor into bone, the system comprising a curved cannulated guide for percutaneous insertion, having a proximal end and a distal end; a flexible drill insertable through the curved guide from the proximal end to the distal end, the flexible drill having a shaft having a flexible portion; and a flexible inserter for inserting a suture anchor into a bore at the anatomical site formed by the flexible drill, the flexible inserter having a shaft having a flexible portion, wherein the flexible portions of both the flexible drill and flexible inserter include a series of discrete, interlocking segments.

Abstract: An endograft is provided for a blood vessel having a branch extending from said blood vessel, including a body having a wall defining a lumen and an exterior surface. The endograft body includes a first portion defining or being made to define a non-circular cross-sectional dimension, and a second portion defining a circular cross-sectional dimension. Modular systems including the endograft and methods for creating endografts according to the disclosure are described also.

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: Systems and method are described for counterbalancing the force required to deform a flexure joint. The system includes an elastically deformable flexure joint, a control joint, and an energy balance system. The control joint is mechanically linked to the flexure joint such that movement of the control joint causes a corresponding deformation of the flexure joint. The energy balance system provides a spring force to aid movement of the control joint and to overcome an elastic force required to deform the flexure joint.

Abstract: In one embodiment, a medical device includes an elongate member and a tissue anchor. The elongate member defines a lumen. The elongate member has a retention member disposed within the lumen. The tissue anchor has a first arm portion, a second arm portion, and a base portion extending between the first arm portion and the second arm portion. The tissue anchor has a first configuration and a second configuration. The first arm portion is substantially linear when the tissue anchor is in its first configuration and the first arm portion is non-linear when the tissue anchor is in its second configuration. The tissue anchor is biased to its second configuration. The tissue anchor is configured to be disposed within the lumen defined by the elongate member such that the retention member engages the tissue anchor to help retain the tissue anchor in its first configuration.

Abstract: A heart valve prosthesis configured to be implanted at cardiac valve annulus located at an interface between a ventricle (LV) and an atrium (LA), the heart valve prosthesis including: a first portion configured for enclosing a plurality of chordae tendineae (CT) in the ventricle (LV) and native valve leaflets (NVL) to which said chordae tendineae are connected, and a second portion including a radially expandable annular member and a prosthetic heart valve anchored to said radially expandable annular member, wherein said first portion is configured to be implanted in the ventricle (LV), and wherein said second portion is configured to be implanted and coupled to the first portion at the cardiac valve annulus.

Abstract: A method for closing a wound in tissue is provided which includes providing a surgical fastener having a plurality of reactive members of a specific binding pair attached on a surface of the surgical fastener, and providing tissue with a plurality of complementary reactive members of the specific binding pair, wherein upon contact of the reactive members on the surface of the surgical fastener with the complimentary reactive members on the tissue, covalent bonds are formed between the reactive members and the complementary reactive members, thus adhering the device to the tissue.

Abstract: A narrow profile surgical ligation clip has two legs with clamping surfaces joined by a hinge near the proximal ends, allowing the clip to reversibly open and close. A locking mechanism is proximal to the hinge to bias or lock the clip closed, including first and second jaw structures spaced on opposite sides of a longitudinal axis of the clip thereby defining a locking space therebetween. In one embodiment, a wedge or buttress body moves by application of an external force applied to a proximal end of the clip towards the hinge to move into the locking space such that one or more outer surfaces or projections of portions of the body fit into or abut against complementary surfaces or other parts of the locking mechanism or clip assembly to bias or lock the clip in a closed position and provide additional closing force to the inner clamping surfaces.

Abstract: A securing device for securing a flexible line to another object. The clip has a working end and a clip end, the former for attachment to the other object and the latter for securing the line. The clip end has two loops and a locking clip. The two loops extend in opposite directions away from the locking clip, and are connected by a crossbar which is perpendicular to and against the locking clip. The locking clip is formed from two parallel shafts, closely spaced together. The line is secured by wrapping it at least twice around the loops, then up over the crossbar and down into the locking clip.