Patent classifications
A61B17/0482
LEAD METHOD OF SUTURING ACUTELY RUPTURED ACHILLES TENDON AND DEVICE USED IN THE LEAD METHOD
Disclosed are a lead method of suturing an acutely ruptured Achilles tendon and a device used in it. The suturing device includes a suture line, guide lines, a clamping instrument and suture needles. As performing suturing, the clamping instrument is inserted into the fascia sheath of Achilles tendon to clamp Achilles tendon, the suture line and the guide lines are made to penetrate Achilles tendon and skin through the threading hole on the clamping instrument by the suture needle, wherein the suture line is located far away from Achilles tendon rupture; the guide lines are used to guide the suture line, so that both ends of the suture line can penetrate Achilles tendon in turn along the guide lines, and the suture line is tightened and knotted on the two ruptured Achilles tendons.
Surgical dissectors configured to apply mechanical and electrical energy
A surgical instrument comprising an end effector is disclosed. The end effector comprises a surgical dissector. The surgical dissector can apply mechanical and/or electrosurgical energy to treated tissue.
Methods of making suture needles with localized regions for bending
A method of making a suture needle having a bendable region includes obtaining a suture needle made of a martensitic alloy having an austenitic transition temperature. The suture needle has a proximal section, a distal section with a sharpened tip, and a bendable region located between the proximal and distal sections. The method includes heating the suture needle to a first temperature that is greater than the austenitic transition temperature of the martensitic alloy and quenching the suture needle to room temperature to harden the martensitic alloy, After heating and quenching, the bendable region of the suture needle is heated locally to a second temperature that is above 800 degrees Celsius, but below the austenitic transition temperature of the martensitic alloy so that the bendable region is softened and made more flexible relative to the proximal and distal sections of the suture needle.
DEVICE FOR CARDIAC SURGERY
A medical device assembly includes a hinge rod having a first portion and a second portion, and a pedestal is coupled to the second portion of the hinge rod, the pedestal having a top surface, and portions of the pedestal cooperate to define a trough that is configured to hold a first portion of a vessel on the top surface of the pedestal. A retainer is movably coupled to the pedestal, and the retainer has a planar member having a lower surface configured to oppose the top surface of the pedestal. A joint member is coupled to the hinge rod, and a clamp assembly is releasably coupled to the joint member such that when the clamp assembly is in a locked configuration, the hinge rod is not repositionable, and when the clamp assembly is in an unlocked configuration, the hinge rod is repositionable.
Suture delivery system
A device is described. The device includes a suture guide and a tissue retracting surface to enable accurate and safe delivery of sutures through tissue.
CLOSING TISSUE OPENINGS
A suture system can comprise a first and a second curved double arm needle, and a needle docking device configured to maintain the first and the second curved double arm needles in alignment with and parallel to one another and at predetermined orientations relative to the needle docking device. The system can include a needle manipulating instrument having a distal portion configured to engage the first and the second curved double arm needles while the first and second curved double arm needles are in the needle docking device, and to maintain the needles in predetermined orientations.
Articulating suture hook
An articulating suture hook for passing or retrieving suture. The suture hook having a handle with a proximal end and distal end. A stiffening tube is fixed to the distal end of the handle extending distally from the handle. A flexible outer tube is fixed to the stiffening tube and extends distally therefrom. A cut portion of the flexible outer tube has a plurality of cuts positioned therealong. In a first configuration, the flexible outer tube extends parallel to or in alignment with the stiffening tube, but in a second configuration, the flexible outer tube is curved at the cut portion. The plurality of cuts may be arranged into two patterns. Each cut arranged in a first pattern is offset at an angle from each cut arranged in a second pattern. The pattern, shape, and size of the cuts determines the movement of the flexible outer tube to the second configuration.
Devices, systems, and methods for repairing soft tissue and attaching soft tissue to bone
Devices, systems and/or methods for fixating soft tissue to bone are provided. In one embodiment, a repair device for fixating soft tissue to bone with a bone anchor includes a soft tissue anchor and one or more flexible members. The soft tissue anchor includes a base with multiple legs extending from the base. The one or more flexible members are coupled to the base and configured to extend from the base to the bone anchor with a fixed length. With this arrangement, the fixed length of the one or more flexible members is configured to maintain a fixed distance between the soft tissue anchor and the bone anchor such that, as the bone anchor is seated into bone, the one or more flexible members pulls the soft tissue anchor down against the soft tissue to fixate the soft tissue to the bone.
Systems and methods for sizing and introduction of soft-tissue allografts
The present disclosure includes systems, methods, kits, and individual tools (e.g., trial sizers and delivery devices) for medical procedures involving a soft-tissue allograft for the correction of skeletal impairments (e.g., misalignments, arthritis, etc.).
ROTARY STITCHING DEVICE
A stitching device includes an end effector having first and second jaw members and first and second pins, a stationary cam, and a rotary cam. The first pin is supported on the first jaw member and the second pin is supported on the second jaw member. The stationary cam defines a first cam slot, and the rotary cam defines a second cam slot. The first and second cam slots receive the first and second pins and are configured to releasably secure one of the first or second jaw members to the rotary cam such that the first and second jaw members rotate about the stationary cam in alternating fashion. During each revolution of the rotary cam, the one of the first or second jaw members rotates with the rotary cam a substantially full revolution while the other of the first or second jaw members remains stationary.