A perfusion bioreactor system has an inner chamber and scaffold with matching porosities to equalize fluid flow through a bioreactor. The scaffold can be fabricated using additive manufacturing or other fabrication techniques to match the geometrical shape of a defect, such as a facial bone anomaly. The inner chamber is fabricated in a similar manner and has an inner cavity matching the shape of the scaffold to create a unified structure when assembled together with the scaffold. By matching the shapes of the scaffold and inner chamber, free space is eliminated within the interior volume of the bioreactor. Stem cells can be flowed through the bioreactor and attached to the scaffold, which are then cultured to grow a tissue graft.

A graft-harvesting instrument and MTP fusion device are disclosed to allow for easy and safe removal of a section of the calcaneus to be used as autograft in the fusion of the MTP joint. The graft-harvesting instrument allows a surgeon to place a barrier between the saw and the vital anatomy on the medial side of the calcaneus. The MTP fusion device allows for the exact placement of the autograft into the MTP joint. The graft-harvesting instrument allows for a very consistent piece of autograft to be harvested. The graft-retaining sleeve component of the MTP fusion device positions that autograft in place for optimum fusion of the MTP joint.

An apparatus and methods are provided for a trephine bone graft harvester for extracting morselized bone from patients. The trephine bone graft harvester includes a bone cutter affixed to an outer hub. The bone cutter comprises a hollow tube having cylindrical wall and a distal cutting edge. A bone graft collector is sheathed within the bone cutter. The bone graft collector includes a distal scoop adjacent to the distal cutting edge of the bone cutter. The distal scoop is configured to move morselized bone away from the distal cutting edge. An inner hub is affixed to the bone graft collector and coupled with the outer hub. The inner hub includes a proximal shank configured to be engaged with a rotary tool suitable for applying torque to the inner hub.

A method for treating cartilage defects including providing a placental membrane preparation that comprises ground or minced placental membranes and optionally, a ground or minced cartilage and/or biocompatible glue, and introducing the preparation to a cartilage defect within a skeletal joint. The cartilage defect may comprise a hyaline cartilage defect, such as a chondral defect, or meniscal defect. The treatment may be provided in combination with other treatments such as marrow stimulation treatments and surgical repair treatments using sutures or other fixation techniques. The preparation promotes the regeneration of cartilage within the skeletal joint.

A denuder, such as a bone stock denuder container, is disclosed. The denuder includes a nozzle and a container body. The nozzle is configured to be fluidically coupled to a source of fluid and to direct a fluid stream. The container body includes curved chamber wall that forms a wash chamber. The wash chamber is configured to receive a bone stock. The nozzle is configured to direct the fluid stream to impact the curved chamber wall.

A shaped cartilage matrix isolated from a human or animal where the cartilage has been crafted to facilitate disinfection, cleaning, devitalization, recellularization, and/or integration after implantation. Also, a process for repairing a cartilage defect with the cartilage matrix. The matrix is in the form of an osteochondral plug including a cartilage cap ad subchondral bone, wherein one or more gaps, slats, bores, or channels extend through the tidemark at the interface between the cartilage cap and the subchondral bone.

A shaped cartilage matrix isolated from a human or animal where the cartilage has been crafted to facilitate disinfection, cleaning, devitalization, recellularization, and/or integration after implantation. Also, a process for repairing a cartilage defect with the cartilage matrix. The matrix is in the form of an osteochondral plug including a cartilage cap ad subchondral bone, wherein one or more gaps, slats, bores, or channels extend through the tidemark at the interface between the cartilage cap and the subchondral bone.

Instrumentation sets and methods for preparing and implanting an osteochondral allograft to a bone lesion. Instrumentation sets include a pair of guide blocks, a recipient guide block and an allograft guide block, for preparing a cavity at the bone lesion matched by a similarly sized and shaped allograft. Guide blocks provide simple and direct techniques for preparing a matching cavity, formed at the bone lesion, to a bone implant, to be secured within the cavity. Methods include use of the instrumentation to restore bone surfaces for any number of sites using any allograft source. In some cases, the bone lesion is in a humeral head and the allograft source is a talus.

A cage device for harvesting bone graft material for use in bone fusion surgery, e.g., a spinal fusion. The device has a chamber configured to contain a slurry of morselized bone and blood that effuses from adjacent bones when the device is placed in a space between the bones, and a bone cutter assembly is inserted into the chamber and operated. In one embodiment, the cutter assembly includes an elongated cannula having a bend at a distal end, and a wire arranged to slide inside the cannula so that a cutting tip of the wire can be set to project a desired distance from the distal end. When the cannula is driven to rotate about its long axis, the wire cutting tip strikes and cuts grooves in the facing surfaces of the bones to produce the mentioned slurry which remains inside the chamber to promote a solid and healthy fusion.

The invention is directed towards a process for implanting a cartilage graft into a cartilage defect and sealing the implanted cartilage graft with recipient tissue by creating a first bore down to the bone portion of the cartilage defect, creating a second shaped bore that is concentric to and on top of the first bore to match the shape and size of the cartilage graft, treating the first bore and the second shaped bore at the defect site with a bonding agent, treating the circumferential area of the cartilage graft with a bonding agent, inserting the cartilage graft into the defect site and wherein the superficial surface of the cartilage graft is at the same height as the surrounding cartilage surface. The first and second bonding agents may be activated by applying a stimulation agent to induce sealing, integration, and restoration of the hydrodynamic environments of the recipient tissue. The invention is also directed towards a process for repairing a cartilage defect and implanting a cartilage graft into a human or animal by crafting a cartilage matrix into individual grafts, cleaning and disinfecting the cartilage graft, applying a pretreatment solution to the cartilage graft, removing cellular debris using an extracting solution to produce a devitalized cartilage graft, implanting the cartilage graft into the cartilage defect with or without an insertion device, and sealing the implanted cartilage graft with recipient tissue. The devitalized cartilage graft is optionally recellularized in vitro, in vivo, or in situ with viable cells to render the tissue vital before or after the implantation. The devitalized cartilage graft is also optionally stored between the removing cellular debris and the recellularizing steps. The invention is further directed toward a repaired cartilage defect.