Abstract: A surgical instrument includes a transducer configured to produce vibrations at a predetermined frequency. An ultrasonic end effector extends along a longitudinal axis and is coupled to the transducer. The ultrasonic end effector comprises an ultrasonic blade and a clamping mechanism. A controller receives a feedback signal from the ultrasonic end effector and the feedback signal is measured by the controller. A lumen is adapted to couple to a pump. The controller is configured to control fluid flow through the lumen based on the feedback signal, and the lumen is located within the ultrasonic end effector.

Abstract: The aim of the invention is to create a device for arranging medical targeting devices, markers, probes or surgical instruments for image-assisted, minimally invasive operations, which has a simple construction and is easy to use. Said device according to the invention has at least one carrier element (1) that can be positioned preferably with an adhesive layer on the surface of the body, and a fine-positioning unit (2). It is proposed that the carrier element (1) comprises at least one interlocking mount (3) for the fine-positioning unit (2) which has a matching complementary shape (3c).

Abstract: Medical leads have one or more openly coiled filars and a distal body coupled to the openly coiled filars. The openly coiled filars provide a lead with compliance and elasticity while the distal body provides the firmness needed for placement and support of the electrodes. The openly coiled filars may transition to a linear distal portion that extends to the distal body, and the distal body may have proximal tines that fold proximally to become adjacent to the linear distal portion of the filars. The openly coiled filars may instead extend to the distal body and the proximal tines may be laterally arced to then fold against the lateral surface of the coiled filars. The tines may fold distally during explantation to allow the distal body to release and exit the body.

Abstract: The present invention relates to detachment mechanisms for delivering and releasing implantable devices into a body lumen. According to certain aspects, systems of the invention include a junction that couples an implantable device to a delivery member. The junction includes an anodic portion and a cathodic portion galvanically coupled to the anodic portion such that the anodic portion corrodes when exposed to an electrolytic fluid, thereby detaching the implantable device from the delivery member without application of energy from an external power source.

Abstract: A valvuloplasty system comprises a balloon adapted to be placed adjacent leaflets of a valve. The balloon is inflatable with a liquid. The system further includes a shock wave generator within the balloon that produces shock waves. The shock waves propagate through the liquid and impinge upon the valve to decalcify and open the valve.

Abstract: A tissue containment system includes a bag body, a member extending from the bag body and defining a channel, and a viewing window. The bag body at least partially defines an interior region configured to contain a loose tissue specimen and defines an opening sized to receive the loose tissue specimen. The bag body is configured such that a first portion of the bag body can be disposed in an abdominal cavity of a patient while a second portion of the bag body extends outside of the patient. The viewing window is at least partially transparent and provides a seal between the interior region of the bag body and an ambient environment. The channel of the member is configured to receive a tissue visualization device that can be used to view the interior region of the containment bag through the viewing window.

Abstract: A z-shaped surgical device including a handle and a rod secured to the handle having: a first elongate segment at a proximal end thereof; a second elongate segment angled with respect to the first segment; and a third elongate segment angled with respect to the second segment. In the illustrative application, the invention provides an arthroscopic meniscus tissue repair suture passer device that penetrates tissue with its distal tip in one direction and utilizes a needle or similar part to penetrate tissue in the opposite direction placing a suture around the torn tissue. The device has an extended z-shaped shape distally that facilitates placement of a suture around torn meniscus tissue with a novel single stroke relative to the prior art.

Abstract: This invention discloses a valved stent for implantation at a dysfunctional or diseased atrioventricular valvular annulus. The valved stent is expandable from a collapsed shape to an expanded shape for minimally invasive delivery and has a low profile at the atrial or superior aspect to achieve improved hemodynamics and offers the capability to fabricate replacement valves having large diameters, The invention also includes a delivery apparatus uniquely designed for implantation of the valved stent and offering the potential for controlled and precise placement of the valved stent at the atrioventricular annulus. The invention also includes methods for use of the above devices and for treating diseased atrioventricular valves.

Abstract: The present invention relates to a device for transcatheter treatment for tricuspid regurgitation and, more particularly, to a device for patients suffering from tricuspid regurgitation. The device for transcatheter treatment for tricuspid regurgitation according to a preferred embodiment of the present invention includes: a hollow coronary sinus tube (22) for engaging into coronary sinus tissue; and a hollow tricuspid valve tube (24) for crossing over tricuspid valve tissue and anchoring at interventricular septum tissue, wherein the coronary sinus tube and the tricuspid valve tube are laterally coupled with each other from upper portions thereof by a predetermined length, and lower portions thereof are separated from each other; and the lower portion of the tricuspid valve tube (24) is provided with a blocking part (30) for blocking a space resulting from incomplete closure of the tricuspid valve.

Abstract: A vascular intervention robot includes a catheter rotation unit for rotating a catheter on an axis parallel to a longitudinal direction of the catheter, a guide wire rotation and supply unit that is provided at one side of the catheter rotation unit and that is provided for transferring a guide wire in a longitudinal direction of the guide wire and for rotating the guide wire on an axis parallel to the longitudinal direction of the guide wire in a state in which the guide wire is inserted in the catheter, a transfer unit for transferring the catheter rotation unit and the guide wire rotation and supply unit in the longitudinal direction of the catheter, and an expanding and contracting unit that is provided at another side of the catheter rotation unit and that is expandable and contractible along the longitudinal direction of the catheter while supporting the catheter when the transfer unit transfers the catheter rotation unit and the guide wire rotation and supply unit in the longitudinal direction of the c

Abstract: A tamponade catheter is disclosed for controlling bleeding from a penetrating or perforating wound in a patient comprising a catheter having an inner catheter lumen with a non-elastic inflatable balloon secured to the catheter in fluid communication with an inner catheter lumen of the catheter. A removable outer sheath overlays the inflatable balloon for inserting the inflatable balloon within the wound of the patient. A bendable flexible stiffening stylet is receivable within the inner catheter lumen of the catheter to aid in navigating the catheter into the wound of the patient. The removable outer sheath and the stylet are removable for inflating the inflatable balloon by an introduction of a fluid through the inner catheter lumen of the catheter for enabling the inflated non-elastic inflatable balloon to create pressure within the wound of the patient to control bleeding therefrom.

Abstract: A prosthesis for repairing a blood vessel, wherein the prosthesis is inserted intraluminally and fixed in the vessel so as to isolate a diseased section thereof and maintain the flow of blood from the vessel to collateral vessels involved the diseased section, and the prosthesis comprises a stent support and a flexible fabric liner of woven material comprising a plurality of concentric layers, wherein each of said layers has a very open fabric web which allows the passage of blood flow through the layers during the installation or the prosthesis but which allows the sealing of layers once the prosthesis is installed. A method is also provided for safe installation of the prosthesis.

Abstract: The invention is suitable for use in medicine for maximally precise, safe and quick positioning a coronary stent in case of simple and complicated anatomical lesions of the coronary bed as well as for stenting renal, visceral arteries. The claimed device comprise a body with a tail portion, a screw rotation wheel, a screw, a slider with a cam, a bush with clip and a rubber coupling provided thereon, a wedge comprised of two members, a spring and a lock button arranged in the body. In preparation to use the device, the coronary stent on the delivery system is first successively introduced into the device whereafter the coronary stent on the delivery system is manually advanced to the affected area of the coronary artery, the delivery system is locked in the device and the stent is positioned within the coronary artery by means of the rotation wheel.

Abstract: An active annuloplasty ring holder having a template that can be folded or pivoted to the side allowing the template to align longitudinally with the handle and enter the patient's chest through a small incision. The holder may include a mechanism to remotely detach sutures fastening the ring to the holder, thereby detaching the ring while avoiding the risk associated with introducing a scalpel into the operating field. A detachment mechanism may include a movable pin actuated by a pull wire that releases a plurality of holding sutures, or a hot wire, knives, or pull wire that severs the sutures. The holder may have a built-in light source for better visualization of the ring inside the heart. The holder may also have an optical means of visualizing the inside of the heart from the proximal end of the handle.

Abstract: The present invention is directed to prostheses including a support structure having a proximal end and a distal end, and a motion limiting member attached to the distal end of the support structure, wherein the motion limiting member is configured to restrict radial expansion of the distal end of the support structure. Methods for delivering the prosthesis are also provided.

Abstract: A robotic arm according to various implementations includes: a tool driver configured to hold a surgical tool; a first section comprising a first end coupled to a base, a second end distal from first end; a first link that includes a motor configured to rotate at least a portion of the first section around a pitch axis; a second link coupled to the first link, the second link including a motor configured to rotate at least a portion of the first section around a roll axis; and a second section comprising: a first end coupled to the second end of the first section, a second end distal from the first end, a first link that includes a motor configured to rotate at least a portion of the second section around a roll axis, a second link coupled to the first link.

Abstract: Provided herein are expandable endoscopic devices. In accordance with certain aspects of an embodiment of the invention, an endoscopic expandable device is disclosed that comprises an expandable jaw at the distal tip, a control wire connected to the jaw, a sheath enclosing the control wire, and a handle connected to the sheath or wire having an actuating trigger. The expandable jaw is configured to allow its delivery in a retracted configuration to a target site within a patient's body through the working channel of an endoscope, after which the jaw may reconfigure to an expanded configuration that is larger than the retracted configuration. This allows the expandable jaw to be easily delivered to the target site while allowing an operable jaw size that is larger than would be allowed if limited to size of the working channel. The endoscopic expandable device may have utility as a clip or as forceps.

Abstract: Disclosed embodiments include apparatuses, systems, and methods for cutting an opening in a tissue wall. In an illustrative embodiment, an apparatus includes an inner cutting member having a first cylindrical body supporting at least one first cutting surface at a distal end. The first cutting surface faces a first rotational direction relative to an axis of the first cylindrical body and has a first cutting edge at an outer periphery of the first cylindrical body. The apparatus also includes an outer cutting member having a second cylindrical body concentrically disposed around the first cylindrical body and supporting at least one second cutting surface at the distal end. The second cutting surface faces a second rotational direction relative to the axis and has a second cutting edge at an inner periphery of the second cylindrical body.

Abstract: The devices and methods described herein relate to clearing of blockages within body lumens, such as the vasculature, by addressing the frictional resistance on the obstruction prior to attempting to translate and/or mobilize the obstruction within the body lumen.

Abstract: Embodiments are directed in part to endovascular prostheses and methods of deploying same. Embodiments may be directed more specifically to stent grafts and methods of positioning and deploying such devices within the body of a patient.