Abstract:
A line lock system may include a line routed through a plate. The plate may have an elongated body with a plurality of passageways. The line is routed to form at least one one-way slide so no knots are required. The system may include filaments routed through the passageways of the plate or around a dogbone feature of the plate. The filaments may be used to toggle the plate after passage through a hole to prevent withdrawal of the plate back through the hole. The system may include a line lock stabilizer or counter-tension tool to stabilize the line lock as the line is adjusted. The system may include a compression limiter to selectively reduce compression in the one-way slide to facilitate adjustment of the line. The line lock stabilizer, counter-tension tool, or compression limiter may be a filament.
Abstract:
A trial system for an implantable joint replacement includes a guide assembly having a baseplate and a guide plate, the guide plate translatable relative to the base plate along a straight path while directly connected to the baseplate. A first adjustment mechanism may selectively control the translational juxtaposition of the guide plate relative to the baseplate. The guide plate may further be rotatable relative to the baseplate around a rotation axis. A second adjustment mechanism may selectively control the rotational juxtaposition of the guide plate relative to the baseplate, and can lock the plates together. The rotation axis may be medially offset from the center of the guide assembly. The guide plate provides in situ positionable cutting guidance for implantation of prosthetic joint components. The system may further include an articulating insert trial mounted on the guide assembly to determine preferred joint alignment and/or optimal positioning of the guide plate.
Abstract:
A trial system for an implantable joint replacement includes a guide assembly having a baseplate and a guide plate, the guide plate rotatable relative to the base plate about a rotation axis extending through the guide plate and the baseplate while directly connected to the baseplate. An adjustment mechanism is actuable to selectively control the rotational juxtaposition of the guide plate relative to the baseplate. The rotation axis may be medially offset from the center of the guide assembly. A single instrument may be used to rotate the guide plate relative to the base plate and lock the plates in the selected juxtaposition. The guide plate provides in situ positionable cutting guidance for implantation of prosthetic joint components. The system may further include an articulating insert trial mounted on the guide assembly to determine preferred joint alignment and/or optimal positioning of the guide plate.
Abstract:
A trial system for an implantable joint replacement includes a guide assembly having a baseplate and a guide plate, the guide plate rotatable relative to the base plate about a rotation axis extending through the guide plate and the baseplate while directly connected to the baseplate. An adjustment mechanism is actuable to selectively control the rotational juxtaposition of the guide plate relative to the baseplate. The rotation axis may be medially offset from the center of the guide assembly. A single instrument may be used to rotate the guide plate relative to the base plate and lock the plates in the selected juxtaposition. The guide plate provides in situ positionable cutting guidance for implantation of prosthetic joint components. The system may further include an articulating insert trial mounted on the guide assembly to determine preferred joint alignment and/or optimal positioning of the guide plate.
Abstract:
A line lock system may include a line routed through a plate. The plate may have an elongated body with a plurality of passageways. The line is routed to form at least one one-way slide so no knots are required. The system may include filaments routed through the passageways of the plate or around a dogbone feature of the plate. The filaments may be used to toggle the plate after passage through a hole to prevent withdrawal of the plate back through the hole. The system may include a line lock stabilizer or counter-tension tool to stabilize the line lock as the line is adjusted, a compression limiter to selectively reduce compression in the one-way slide to facilitate adjustment of the line, means for adjusting the line, or a line cutter.
Abstract:
Knee prosthesis instrumentation including an insertion tool and a removal tool. The insertion tool may include an offset to provide clearance from a femoral component of the knee prosthesis. The removal tool may be wedge shaped to at least partially encircle a post of the knee prosthesis for removal. A mallet may be used with the instruments to provide additional force for prosthesis insertion or removal. A slide hammer may be incorporated into the instruments themselves.
Abstract:
A trial system for an implantable joint replacement includes an articular insert having an insert body and an insert post captive to the insert body. The insert post is translatable relative to the insert body while remaining captive to the insert body. An aperture on the insert body forms a path, which may be arcuate, along which the insert post can translate. An axis of rotation about which the insert post translates passes through the insert body, and may be medially offset from the center of the body. A flexible element may connect the insert post to the insert body. In one method of use, the trial system is engaged with a femoral component and a tibial component during a prosthetic total knee joint implantation procedure to determine selection of an implantable articular insert which provides knee joint articulation closely matching the articulation of a natural knee.
Abstract:
A trial system for an implantable joint replacement includes a guide assembly having a baseplate and a guide plate, the guide plate translatable relative to the base plate along a straight path while directly connected to the baseplate. A first adjustment mechanism may selectively control the translational juxtaposition of the guide plate relative to the baseplate. The guide plate may further be rotatable relative to the baseplate around a rotation axis. A second adjustment mechanism may selectively control the rotational juxtaposition of the guide plate relative to the baseplate, and can lock the plates together. The rotation axis may be medially offset from the center of the guide assembly. The guide plate provides in situ positionable cutting guidance for implantation of prosthetic joint components. The system may further include an articulating insert trial mounted on the guide assembly to determine preferred joint alignment and/or optimal positioning of the guide plate.
Abstract:
A trial system for an implantable joint replacement includes an articular insert having an insert body and an insert post captive to the insert body. The insert post is translatable relative to the insert body while remaining captive to the insert body. An aperture on the insert body forms a path, which may be arcuate, along which the insert post can translate. An axis of rotation about which the insert post translates passes through the insert body, and may be medially offset from the center of the body. A flexible element may connect the insert post to the insert body. In one method of use, the trial system is engaged with a femoral component and a tibial component during a prosthetic total knee joint implantation procedure to determine selection of an implantable articular insert which provides knee joint articulation closely matching the articulation of a natural knee.
Abstract:
A knee prosthesis including femoral and tibial implants, a tibial insert and a cam post assembly. The femoral implant is secured to a femur and has a cam feature and condyles. The tibial implant is secured to a tibia. The tibial insert has articulating surfaces that match the contours of the condyles of the femoral implant, and may have a medial boss that aligns with the tibial implant to provide rotation about a medially displaced rotation axis. A cam post is secured to the tibial implant and passes through a channel of the tibial insert. A motion limiting structure provides limits to motion between the tibial insert and the tibial baseplate. The cam post assembly interacts with the femoral implant cam feature and allows more anatomically correct rollback and femoral external rotation during knee flexion, and varus/valgus support to the femur.