A device for cardiac surgery is disclosed, having a) a plurality of pairs of suture guides spaced about the frame; b) a plurality of suture tubes, with one suture tube corresponding to each pair of suture guides; c) a plurality of snares, each corresponding to and passed through one of the plurality of suture tubes so that a handle at one end of the snare protrudes from a proximal end of the corresponding suture tube and a snare loop at another end of the snare protrudes through a distal end of the corresponding suture tube, and wherein the snare loop further protrudes through one of the suture guides in the corresponding pair of suture guides; and d) a plurality of sutures, each corresponding to one of the pairs of suture guides and coupled to the suture guide in the corresponding pair of suture guides which does not have the snare loop passing through it.

A surgical site retractor is configured to retract tissue, such as in an intercostal procedure. The retractor may be formed from non-radiopaque material for improved monitoring via x-ray imaging. The retractor may have a rigid retractor and a soft tissue retractor, where the rigid retractor has a plurality of legs and the soft tissue retractor extends between the legs to prevent soft tissue from extending between said legs. The retractor may have a bendable arm with an implement holder, such as distal cuff or clip adapted to resiliently hold an implement such as a tube of an elongated port-access device. A method involves partly installing the surgical site retractor, expanding the surgical site retractor, deploying the surgical implement from outside the body through the incision and into the patient, resiliently capturing the implement with the holder of the arm, and bending the arm to hold the implement in a desired position.

A retractor system includes a retractor with an oximeter sensor at its tip and a force sensor coupled to the retractor. The retractor system also includes a system unit which can send signals to and receive signals from the oximeter sensor via optical fibers. The oximeter sensor measures oxygen saturation of a tissue being retracted by the retractor, and the force sensor measures an amount of force that is applied to the retracted tissue by the tip of the retractor. Another retractor system has a closed loop control arrangement with a positioning mechanism which moves the retractor based on measurements of the sensors.

A surgical stabilizer arm includes a reusable base portion and a disposable arm portion. The articulating links that enable the arm to be positioned into arbitrary trajectories are included the disposable portion, thus eliminating the need to clean between the links after a surgical procedure. The disposable portion also includes a tool attachment mechanism and a cable. The reusable portion includes a retractor clamping mechanism, a top plate, a T-shaped base post, a main body, a nosepiece, a threaded drawbar, a thrust bearing assembly, and a threaded handle that can extend or retract the drawbar when rotated. The threaded drawbar may include a slot into which an end of the cable can be inserted, which allows tension to be applied to the cable when the handle is rotated to pull the drawbar into the body of the reusable portion and lock the articulating links in place.

A hands-free mitral papillary muscle exposure device provides a clear view of the papillary muscles, including the pathology of the leaflets and chordae tendineae of a mitral valve apparatus, and comprises a retractor device comprises two arm members pivotally connected to one another which can be manually spread and adjusted about a pivot point to a desired arrangement relative to the mitral valve apparatus to prevent injury to surrounding muscle and tissue during an operative procedure. Each arm member includes a respective downwardly extending longitudinal projection to hold one of the anterior and posterior leaflets adjacent to said arm member when the retractor device is positioned relative to the mitral valve apparatus. The longitudinal projection on the anterior side of the retractor device is longer than the corresponding longitudinal projection on the posterior side to accommodate the longer size of the anterior leaflet in comparison with the posterior leaflet.

A suturing device is disclosed. The suturing device has a guide tip. The guide tip has first and second framing arms that define a viewing port from a first orientation. The guide tip also has proximal and distal ends of the guide tip which, with the first and second framing arms, define a tissue bite area from a second orientation. The suturing device also has a ferrule holder located in the distal end of the guide tip and centered relative to the first orientation. The suturing device further has a needle movable within the guide tip along a path through the tissue bite area and centrally viewable in the viewing port relative to the first orientation.

The present application relates to a double blade for a surgical retractor having a base body with a substantially cylindrical mounting mandrel for mounting the double blade on a surgical retractor, and at least two blade elements that are so mounted on the base body as to be rotatable and/or displaceable through at least a certain angular range with respect to the base body. Moreover, the present application relates to a blade arrangement in which a double blade is connected to a connecting element of a further double blade, or a single blade. In this case, the at least one double blade or, optionally, the single blade is rotatable with respect to the connecting element. In addition, the application relates to a retractor with a double blade, a blade arrangement or a blade assembly comprising double blades and a blade arrangement.

Devices, apparatus, and methods for catheter-based repair of cardiac valves, including transcatheter-mitral-valve-cerclage annuloplasty and transcatheter-mitral-valve reapposition. In particular, a target and capture device is provided for guiding a cerclage traversal catheter system through a cerclage trajectory, particularly through a reentry site of the cerclage trajectory. The target and capture device provides the user with a target through which the cerclage traversal catheter system must be guided, particularly under imaging guidance, so as to properly traverse the cerclage trajectory at any desired location, particularly at a reentry site. The target and capture device can, further, ensnare and externalize the cerclage traversal catheter system.

Methods and devices described herein facilitate diaphragm entry for posterior access of body organs.

A device for treating heart failure in a patient. The device comprising a body, at least one passage through the body, at least one one way valve in the passage and a mounting means adapted for mounting the body in an opening provided in the patient's atrial septum. In use, the device is oriented such that, when the patient's left atrial pressure exceeds the patient's right atrial pressure by a predetermined amount, the one way valve(s) opens to allow blood flow through the passage(s) from the left atrium to the right atrium to thereby reduce the left atrial pressure.