A system of prosthetic implants for a total knee replacement procedure is provided. The system includes a tibial component of a knee joint implant, a tibial insert configured to be positioned against the superior side of the platform of the tibial component, a first femoral component of a knee joint implant, and a second femoral component of a knee joint implant.

An intervertebral implant for insertion into an intervertebral disc space between two adjacent vertebral bodies of a human or animal spine. The intervertebral implant has an implant top side, which defines a first vertebral body abutment face for abutting against a first vertebral body, and an implant bottom side, which defines a second vertebral body abutment face for abutting against a second vertebral body. The intervertebral implant comprises a frame structure with at least two support elements. The at least two support elements extend from the implant top side to the implant bottom side. The at least two support elements define support element longitudinal axes, which run transversely, in particular perpendicularly, to the first and/or second vertebral body abutment face.

A dilation introducer for orthopedic surgery is provided for minimally invasive access for insertion of an intervertebral implant. The dilation introducer may be used to provide an access position through Kambin's triangle from a posterolateral approach. A first dilator tube with a first longitudinal axis is provided. An access cannula may be introduced over the first dilator tube. A drill may be inserted through the access cannula and used to perform a foraminoplasty. Surgical instruments may pass through the access cannula to operate on an intervertebral disc and/or insert an intervertebral implant.

An orthopedic system for delivery of a therapeutic agent to a bone includes an elongate stem adapted to be inserted into an intramedullary canal, an inlet configured to receive the therapeutic agent, and one or more outlets configured to deliver the therapeutic agent to the bone. The elongate stem may comprise one or more protrusions to engage the bone, and one or more channels extending longitudinally therein, fluidly coupled to the inlet. The therapeutic agent flows from the inlet through the one or more channels and exits into the intramedullary canal through the one or more outlets. The system may be configured to allow one or more dimensions of the system to be adjusted to accommodate the anatomy of a patient.

A glenoid implant includes a body, a plurality of fins, a collet, and a plug. The body has a central aperture therethrough and a plurality of slots. Each of the plurality of fins are coupled with a respective one of the plurality of slots of the boss of the body such that each of the plurality of fins is configured to move from a first generally inward position towards a second generally outward position. The collet including an interior threaded bore and a plurality of deflectable arms. The plug includes a threaded portion and a tip portion configured to engage with and cause the plurality of deflectable arms of the collet to move and cause the plurality of fins to move from the first generally inward position towards the second generally outward position, thereby aiding in securing the body to a scapula of a patient.

In a tibial component, an engagement mechanism configured to engage a tibial block and a tibial tray includes a recessed portion that is disposed in a lower surface, is non-penetrating, and includes an overhanging portion protruding inward more on an opening side than on a bottom portion side in at least a part of an inner wall; and a projecting portion that protrudes from the tibial block to the lower surface side, and includes a protruding part configured to engage with the overhanging portion.

Exemplary cutting and alignment guide assemblies for use in microsurgical, plastic surgical, otolaryngological, maxillofacial, orthopedic, dental, or other surgical procedures include a first section configured to engage a first bone graft section, a second section configured to engage a second bone graft section, a first fixation mechanism configured to couple the first section with the first bone graft section, and a second fixation mechanism configured to couple the second section with the second bone graft section. The first section and the second section can be coupled via a hinge mechanism. Neo-mandible assemblies for implantation at a native mandibular defect of a patient can include a cutting and alignment guide coupled with one or more bone graft sections. In some cases, bone graft sections include bone segments from a fibula of the patient.

A knee joint prosthesis may be for implantation in a knee of a patient. The knee prosthesis may comprise a tibial component configured to be implanted on the tibia and a femoral component configured to be implanted on the femur. The femoral component may comprise a medial condyle with a medial articulation surface and a lateral condyle with a lateral articulation surface. The medial articulation surface and the lateral articulation surface may be shaped substantially symmetrically to each other across a femoral component plane bisecting the femoral component. The tibial component may comprise an articulation surface with a medial articulation side configured to articulate with the medial articulation surface and a lateral articulation side configured to articulate with the lateral articulation surface. The medial articulation side and the lateral articulation side may be shaped substantially asymmetrically to each other across a tibial component plane bisecting the tibial component.

Disclosed herein is an implant. The implant can include a body and a plurality of fixation members. The body can define an articular surface and a bone engaging surface opposite the articular surface. The bone engaging surface can define a groove that separates a first section of the bone engaging surface from a second section of the bone engaging surface. The plurality of fixation members can extend from the bone engaging surface.

An orthopedic system for delivery of a therapeutic agent to a bone includes an elongate stem adapted to be inserted into an intramedullary canal, an inlet configured to receive the therapeutic agent, and one or more outlets configured to deliver the therapeutic agent to the bone. The elongate stem may comprise one or more protrusions to engage the bone, and one or more channels extending longitudinally therein, fluidly coupled to the inlet. The therapeutic agent flows from the inlet through the one or more channels and exits into the intramedullary canal through the one or more outlets. The system may be configured to allow one or more dimensions of the system to be adjusted to accommodate the anatomy of a patient.