A61F2002/30565

Modular transdermal compress device

A modular transdermal assembly configured to couple an external prosthetic device to a bone stump. The assembly includes a modular transdermal portion and a bone fixator. The modular transdermal portion includes an interface portion configured to couple with the external prosthetic device. The bone fixator is configured to be secured to the bone stump and couple with the modular transdermal portion to retain the modular transdermal portion relative to the bone stump.

Implant evaluation in prosthesis installation
10849766 · 2020-12-01 ·

A system, method, and computer program product for allowing any surgeon, including those surgeons who perform a fewer number of a replacement procedure as compared to a more experienced surgeon who performs a greater number of procedures, to provide an improved likelihood of a favorable outcome approaching, if not exceeding, a likelihood of a favorable outcome as performed by a very experienced surgeon with the replacement procedure, such as by understanding the prosthesis installation environment (e.g., cup/cavity interface) and to provide intelligent and interactive tools and methods to standardize the installation process and provide feedback regarding a quality of insertion/installation. Force sensing is included to aid in quantifying installation of an implant, particularly a cup into a pelvic bone.

SURVEYING TIBIAL TRIALS FOR KNEE ARTHROPLASTY
20200368040 · 2020-11-26 · ·

A system and process for performing orthopedic surgery is provided that uses a tibial trial system in total knee arthroplasty for assessing optimal internal-external rotation and posterior tibial slope, and for measuring the rotation of a tibial trial throughout flexion-extension to determine and mark the best position for the final tibial component. The tibial trial system determines the internal-external location on a patient specific basis with improved component placement well within the present manual methods. One particular advantage to the tibial trial system is to assess the natural internal-external rotation that the tibial component will experience relative to the femoral component during flexion-extension as opposed to simply recording and balancing forces on a static tibial trial. The invention disclosed herein may also be adapted to be used with a computer assisted surgical device. Such surgical devices include active, semi-active, and haptic devices as well as articulating drill and saw systems.

CONVERTIBLE GLENOID IMPLANT
20200368031 · 2020-11-26 ·

A glenoid implant including a base plate and an articular component. The base plate can include a body and a support structure extending from a distal surface of the body. The body can include a plurality of openings. The articular component can be configured to removably couple to the base plate. The articular component can include a recessed portion configured to at least partially receive the body of the base plate. At least one engagement structure can protrude from a distal facing surface of the recessed portion. Each engagement structure can correspond to one of the plurality of openings in the body. A distal face of the articular component surrounding the recessed portion can be configured to abut the subchondral bone.

Process for introducing a stabilizing element into a vertebral element

A process for introducing a stabilizing element into a vertebral column, in which the stabilizing element is introduced in such a manner that the stabilizing element connects two adjacent vertebral bodies to one another.

Facet joint replacement devices

Devices and systems can be used to treating spinal conditions. For example, this document describes artificial facet joint systems that can be implanted to treat spinal conditions while facilitating normal stability and motions of the spine. Such systems and methods can be used to treat spinal conditions such as, but not limited to, spondylosis, vertebral fractures, and the like.

Spring Retained Femoral Augment
20200352724 · 2020-11-12 ·

An orthopedic system that includes a first augment that has a body and a first biasing member projecting from the body. The body has a first and second face. The first and second faces are separated by a thickness of the augment. The system also includes a femoral prosthesis that has an articular side that defines condylar portions and a bone-facing side opposite the articular side. The bone facing side defines an augment opening that is sized to receive the augment therein. When the first augment is received within the augment opening, the first biasing member presses directly against the femoral prosthesis so as to retain the body within the augment opening.

Spinal fixation system

A spinal fixation system includes an expandable disc replacement body and an adjustment mechanism. The expandable disc replacement body includes a first wall, a second wall, a hinge connecting the first wall and the second wall, and a first bone-screw receiving section at a proximal end of the first wall. The adjustment mechanism is positioned between the first wall and the second wall, and an angle between the first wall and the second wall can be varied by movement of the adjustment mechanism.

STRENGTH AND FATIGUE LIFE IMPROVEMENTS FOR ACTIVE BONE AND JOINT STABILIZATION DEVICES

Bone and joint stabilization devices or systems are described that include multiple-layer bodies. The approach offers dramatically improved fatigue life as compared to one-piece spring members that are otherwise similar or comparable. Coordinated improved-strength anchor embodiments, anchor loading tools and methods of use are also described.

Bone fusion system

A method and system for performing bone fusion and/or securing one or more bones, such as adjacent vertebra, are disclosed. The screw includes a threaded distal piece fixedly attached connected to an inner post. Both the inner post and the proximal piece have non-cylindrical receptacles at their proximal ends for engagement with driving tools. Independent rotation of the proximal piece and the distal piece enables for compression or decompression to modify the gap between two bones or bone fragments. During use, the distal piece of the bone screw is placed at least partially within a distal bone, the proximal piece is placed at least partially within a proximal bone, and one of two pieces is rotated while the other is held in a fixed position, causing movement of the proximal and distal bones relative to each other.