44 results about "Tendon grafting" patented technology

Devices formed of or including biocompatible polyhydroxyalkanoates are provided with controlled degradation rates, preferably less than one year under physiological conditions. Preferred devices include sutures, suture fasteners, meniscus repair devices, rivets, tacks, staples, screws (including interference screws), bone plates and bone plating systems, surgical mesh, repair patches, slings, cardiovascular patches, orthopedic pins (including bone filling augmentation material), adhesion barriers, stents, guided tissue repair/regeneration devices, articular cartilage repair devices, nerve guides, tendon repair devices, atrial septal defect repair devices, pericardial patches, bulking and filling agents, vein valves, bone marrow scaffolds, meniscus regeneration devices, ligament and tendon grafts, ocular cell implants, spinal fusion cages, skin substitutes, dural substitutes, bone graft substitutes, bone dowels, wound dressings, and hemostats. The polyhydroxyalkanoates can contain additives, be formed of mixtures of monomers or include pendant groups or modifications in their backbones, or can be chemically modified, all to alter the degradation rates. The polyhydroxyalkanoate compositions also provide favorable mechanical properties, biocompatibility, and degradation times within desirable time frames under physiological conditions.

A bioabsorbable implantable device for replacing sutures in construction of a composite graft in ligament replacement surgery. In certain embodiments the device has a female component and a male component where the female component receives and secures the male component. In other embodiments the components of the device are in the shape of a rivet or a staple. The bioabsorbable implantable devices can be used for securing tendon grafts to bone blocks and for holding together the fibers of the tendon graft when the bone-tendon-bone graft is inserted into a patient during surgery. The bioabsorbable implantable device may also be part of a package for use in surgery. The package includes a sterile container for holding at least a graft that is of a predetermined length and width. The package may also include bone blocks. The package is marked as to the graft size including the width and the length of the graft. The graft and the bone blocks may be autogenous, allogenic or constructed from man-made materials.

A method for anchoring autologous or artificial tendon grafts in bone is provided. In one embodiment, the method includes affixing a stabilizing element in bone; and placing the stem of an insertion element therein. A tendon graft may be secured to the insertion element either before or after its placement in the stabilizing element. Two such anchors may be linked with one or multiple grafts, in either a two-ply or four-ply arrangement.

An anchor assembly for autologous or artificial tendon grafts comprises an insertion element and a stabilizing element. The insertion element has a stem and a head containing an aperture large enough to receive a graft. The stabilizing element is adapted to be embedded in bone, and comprises a sleeve with a cavity arranged to receive and hold the insertion element stem. In use, the stabilizing element is affixed in the bone, and the stem of the insertion element is placed therein. A tendon graft may be secured to the insertion element either before or after its placement in the stabilizing element. Two such anchors may be linked with one or multiple grafts, in either a two-ply or four-ply arrangement.

An expanding plug for tendon fixation features a two-part system in which an expansion pin fits inside a fixation sleeve. The fixation sleeve is configured to expand diametrically to achieve interference fixation of a graft tendon inside of a bone tunnel. Fixation sleeve expansion is urged by a two-step engagement of the expansion pin. The tendon graft is assembled to the expanding bolt and situated within a bone tunnel. Passing suture is used to pull a joint-line end of the expansion pin into the tunnel to partially expand the fixation sleeve at the joint-line end. Pulling a graft end of the expansion pin toward the joint line expands the fixation sleeve to place the expanding plug in the fully deployed configuration.

Methods of generating and expanding proliferative, multipotent connective tissue progenitor cells from adult stem cells are provided. Also provided are methods of generating functional tendon grafts in vitro and bone, cartilage and connective tissues in vivo using the isolated cell preparation of connective tissue progenitor cells.

A device serves for blocking a tendon graft in a drilled hole. An element is connected to said tendon graft which can be expanded radially. The element has a cylindrical body which is divided by an oblique cut into two wedge-shaped bodies initially connected to one another via a predetermined break point.

A tapered tendon graft anchor employed during a tendon graft reconstruction surgical procedure. The anchor of the invention comprises a “hair-pin” configuration formed of a loop and two opposing leafs. Each of the leafs include inwardly extending teeth in facing alignment with each other. The outer surfaces of the leafs are tapered to a frustro-conical shape. A harvested tendon with a bone block at one end is positioned with a cavity defined by the loop of the “hair pin” configuration with the tendon positioned between the inwardly extending teeth of the leafs. When the anchor is positioned within a hole in the bone of the joint whose ligament is to be reconstructed, the tendon is tightly grasped by the anchor to securely anchor the tendon in the hole allowing the bone block to be grafted within the hole.

The invention discloses a quick repair method for continuous collapse of an RC framework structure. The invention relates to a repair method for the continuous collapse of the RC framework structure, and aims to solve the problems of large economic losses and long reconstruction cycle caused by the situation that when buildings are continuously collapsed, the whole structure needs to be dismantled. The method is realized through the following steps: I, building supporting systems each of which consists of a jack, a supporting pier and a steel base plate; II, supporting the bottoms of damaged columns and the bottoms of damaged beams with the built steel base plates; III, jacking up a collapsed structure to the elevation of a structure which is not collapsed; IV, supporting the bottom of each layer of the damaged beams above the damaged columns with the steel base plates; V, striking concrete at the region of the end part of a damaged beam till the concrete is crushed; VI, straightening a reinforcing bar which is not cracked in the damaged beam, and transecting a cracked reinforcing bar; VII, repairing the cracked reinforcing bar according to a tendon grafting method; VIII, bundling hoop tendons, supporting molds, casting grouting materials, and dismantling molds; IX, repairing the damaged columns; X, removing supporting piers, the jacks, the base plates, and the like under the damaged beams. The method disclosed by the invention is applied to the field of the continuous collapse of the RC framework structure.