The invention relates to an implant (1) for introducing into a patient, having an implant body that is at least partially resorbable and is porous at least in some regions and that is made of a ceramic carrier material (2), the carrier material being provided with a donor material (3) that delivers ions to influence the patient's cellular metabolism in the implanted state, the carrier material (2) being interspersed with the donor material (3). The invention also relates to a method for producing an implant (1) of said type.

Acetabular implant and method for its manufacture, wherein the implant has a bone side with a contact surface to be fixed against the bone of the hip socket. A plastically deformable zone with an open porous structure connects to the contact surface, the zone being formed by a three-dimensional structure composed of strut elements with opposite ends, wherein these strut elements are connected at their ends in nodes. The zone is made of a material having an elongation at break of at least 15%.

A prosthetic implant shaped as a portion of a human skeletal structure and including a contact and delivery portion shaped as a porous structure, in particular as a trabecular type structure, suitable for receiving a medical substance and configured to be arranged in contact with a bone of a patient during an operating configuration of the prosthetic implant and a support portion, coupled to the contact and delivery portion, including a plurality of ducts each having at least one inlet section, made at an operative part of the prosthetic implant that can be accessed from the outside by the surgeon in the operating configuration, and at least one outlet section which opens into the contact and delivery portion. The contact and delivery portion is configured to deliver the medical substance evenly onto the bone when the medical substance is injected through at least one duct of said plurality of ducts during the operating configuration.

An intervertebral spacer is disclosed having a main body and an articulating component that is pivotally mounted within an opening of the main body. The intervertebral spacer is designed to be manufactured using an additive manufacturing process without the use of any frangible support material between a main body of the intervertebral spacer and an articulating component of the intervertebral spacer. To this end, an article of manufacture is provided in which supports are formed prior to forming intervertebral spacer. The supports are configured to support the main body and the articulating component such that they can be separately, but simultaneously manufactured using an additive manufacturing process atop the supports, without the need for any frangible support material therebetween.

Bone implants, including methods of use and assembly. The bone implants, which are optionally composite implants, generally include a distal anchoring region and a growth region that is proximal to the distal anchoring region. The distal anchoring region can have one or more distal surface features that adapt the distal anchoring region for anchoring into iliac bone. The growth region can have one or more growth features that adapt the growth region to facilitate at least one of bony on-growth, in-growth, or through-growth. The implants may be positioned along a posterior sacral alar-iliac (“SAT”) trajectory. The implants may be coupled to one or more bone stabilizing constructs, such as rod elements thereof.

A method of treating a patient in need of an orthopedic implant is described. The method includes obtaining the T-score or bone density of the patient's native bone at a site of implantation, said T-score or bone density being determined by a DEXA scan or other means of determining a T-score or bone density. The method further includes selecting an orthopedic implant that has about the same density as the native bone at the site of implantation, and implanting the orthopedic implant at the site of implantation.

A method for manufacturing an implantable device is provided. The method includes laser nano-texturing a titanium surface. The method further includes applying an aqueous silver ion solution to form a silver ion complex on the nano-textured titanium surface. The method also includes reducing, using laser-assisted photocatalytic reduction, the silver ion complex to silver ion particles which are immobilized on the nano-textured titanium surface.

In one aspect, an implant for replacing subject tissue includes a nonbiologic portion and a biologic portion grown on the nonbiologic portion. The biologic portion may be grown on the nonbiologic portion before being implanted in the subject. The nonbiologic portion may comprise a porous metal substrate (e.g., scaffolding). The nonbiologic portion may be formed by 3D printing (i.e., additive manufacturing). The nonbiologic portion may be patient-specific. A robot may be used to shape the implant before implantation and/or to shape bone being replaced/resurfaced.

In one embodiment of the disclosure, a prosthetic bone implant includes a prosthesis and a tissue attachment structure connected to the prosthesis. The tissue attachment structure includes a connective structure connected to the prosthesis and an interface structure connected to the connective structure. The interface structure is configured for attachment of tissue thereto. When the interface structure is subject to tension, the connective structure changes in shape.

A reverse shoulder system can include, for example, a glenoid baseplate comprising a longitudinal axis, the glenoid baseplate further including a stem and a central channel within a sidewall of the stem. The stem can include a longitudinal axis. The longitudinal axis of the glenoid baseplate can be angled with respect to the longitudinal axis of the stem, wherein the longitudinal axis of the glenoid baseplate is not perpendicular with respect to the longitudinal axis of the stem. Other components including a glenosphere, tools, and methods of use are also disclosed.