351 results about "Articularis genus" patented technology

The invention relates to a surgical implant that provides an artificial diarthroidal-like joint, suitable for use in replacing any joint, but particularly suitable for use as an intervertebral disc endoprosthesis. The invention contains two rigid opposing shells, each having an outer surface adapted to engage the surfaces of the bones of a joint in such a way that the shells are immobilized by friction between their outer surfaces and the surfaces of the bone. These outer surfaces are sufficiently rough that large frictional forces strongly resist any slippage between the outer surface and the bone surfaces in the joint. They may be convex, and when inserted into a milled concavity, are immediately mechanically stable. Desirably, the outer surfaces of the shells are adapted to allow for bony ingrowth, which further stabilizes the shells in place. The inner surfaces of the shells are relatively smooth, and adapted to slide easily across a portion of the outer surface of a central body disposed between the shells. The central body has a shape that cooperates with the shape of the inner surface of the shell so as to provide a range of motion similar to that provided by a healthy joint. A flexible sheath extends between edges of the opposing shells. The inner surface of this sheath, together with the inner surfaces of the rigid shells, defines a cavity encasing the central body. At least a portion of this cavity is filled with a fluid lubricant, further decreasing the frictional force between inner surfaces of the shell and the surface of the central body.

The invention relates to a surgical implant that provides an artificial diarthroidal-like joint, suitable for use in replacing any joint, but particularly suitable for use as an intervertebral disc endoprosthesis. The invention contains two rigid opposing shells, each having an outer surface adapted to engage the surfaces of the bones of a joint in such a way that the shells are immobilized by friction between their outer surfaces and the surfaces of the bone. These outer surfaces are sufficiently rough that large frictional forces strongly resist any slippage between the outer surface and the bone surfaces in the joint. They may be convex, and when inserted into a milled concavity, are immediately mechanically stable. Desirably, the outer surfaces of the shells are adapted to allow for bony ingrowth, which further stabilizes the shells in place. The inner surfaces of the shells are relatively smooth, and adapted to slide easily across a portion of the outer surface of a central body disposed between the shells. The central body has a shape that cooperates with the shape of the inner surface of the shell so as to provide a range of motion similar to that provided by a healthy joint. A flexible sheath extends between edges of the opposing shells. The inner surface of this sheath, together with the inner surfaces of the rigid shells, defines a cavity encasing the central body. At least a portion of this cavity is filled with a fluid lubricant, further decreasing the frictional force between inner surfaces of the shell and the surface of the central body.

Disclosed herein is a method of computer generating a three-dimensional surface model of an arthroplasty target region of a bone forming a joint. The method may include: generating two-dimensional images of at least a portion of the bone; generating an open-loop contour line along the arthroplasty target region in at least some of the two-dimensional images; and generating the three-dimensional model of the arthroplasty target region from the open-loop contour lines.

Methods of stabilizing the sacroiliac joint by placing an expandable device in the joint to generate laterally opposing forces against the iliac and sacral surfaces of the SI joint to securely seat the device in a plane generally parallel to the SI joint. The expandable device is coated with or otherwise contains a bone material to promote fusion of the joint. The expandable device used in methods of the present invention can be, for example, an expandable cage, a balloon, a balloon-expandable stent or a self-expanding stent.

The invention discloses methods and devices for repairing, replacing and / or augmenting natural facet joint surfaces and / or facet capsules. A facet joint restoration device of the invention for use in a restoring a facet joint surface comprises: a cephalad facet joint element comprising a flexible member adapted to engage a first vertebrae and an artificial cephalad joint; and a caudad facet joint element comprising a connector adapted for fixation to a second vertebrae and an artificial caudad joint adapted to engage the cephalad facet joint. In another embodiment, the invention discloses a facet joint replacement device for use in replacing all or a portion of a natural facet joint between a first vertebrae and a second vertebrae comprising: a first cephalad facet joint element having a fixation member adapted to engage a lamina or spinous process of the first vertebrae and a first caudad facet joint element, the first caudad facet joint element comprising a first caudad connector adapted to fixate to the second vertebral body and an artificial caudad facet surface adapted to engage with the cephalad facet joint element.

An orthopedic implant includes at least one circular body. The at least one circular body defining an outer surface configured to engage at least one articular surface of a sacro-iliac joint along a plane substantially parallel to the articular surface.

A patellar alignment device for determining the position of a patella prosthesis. The device comprises two components-a baseplate and a mobile component which is preferably magnetically attached to the baseplate. During a surgical procedure to replace the knee, the baseplate is temporarily attached to the back of the patella. The baseplate may contain spikes or prongs to secure it to the patella. The baseplate further includes a series of slots for marking the patella. The mobile component resembles a patella and is placed on the baseplate. The patella with the alignment device in place is then placed in position on the knee and trialed. Because the mobile component is free to move on the baseplate, it finds the position that is most amenable to a natural knee movement. The alignment device is then exposed and the patella is marked at the position of the mobile component. Since the baseplate contains a series of slots, the patella can be easily marked at several locations around the mobile component. The entire patella alignment assembly is then removed and the final prosthetic device can be inserted at the marked location.

A cutting tool is provided with an arcuate cutting blade that preferably engages a guide tool to create a curved resected surface during an arthorplasty procedure. In one embodiment, a depth of the cutting blade is sufficient to permit the simultaneous creation of resected surfaces on two bones that articulate, such as both the femor and the tibia for a given condyle, without the need to reposition the guide or the leg. In another embodiment, a cutting member has a generally rectangular cross-section along a longitudinal axis with a first and second surface having cutting teeth defined thereon and a third and fourth surface adapted to interface with a cutting guide positioned proximate the bone. In this embodiment, the cutting tool can resect the bone in two different directions without reorienting the cutting member.

An artificial knee joint that includes a femoral component with a specially shaped bearing surface and a tibial component, whose surface interacts with the femoral surfaces. The interaction provides for the motion and stability characteristics of the anatomic knee. The interaction between the femoral and tibial surfaces is such that as the knee is flexed to maximum, the femoral component moves posteriorly on the tibial surface, more so on the lateral side than on the medial side. This is accomplished by the interaction of a projecting tibial post inside a cupola in the center of the femoral component, and by the saggital radius on the medial side being smaller than that on the lateral side. The prevention of anterior sliding of the femur on the tibia in early flexion is accomplished by the interaction between a distal-anterior recess on the medial side of the femur and an apposing raised pad on the tibial surface. Rotational laxity at all angles is allowed by the presence of only one recess pad and by non-conforming femoral-tibial surfaces on the lateral side.

Systems and methods for providing deeper knee flexion capabilities, more physiologic load bearing and improved patellar tracking for knee prosthesis patients. Such systems and methods include (i) adding more articular surface to the antero-proximal posterior condyles of a femoral component, including methods to achieve that result, (ii) modifications to the internal geometry of the femoral component and the associated femoral bone cuts with methods of implantation, (iii) asymmetrical tibial components that have an unique articular surface that allows for deeper knee flexion than has previously been available, (iv) asymmetrical femoral condyles that result in more physiologic loading of the joint and improved patellar tracking and (v) modifying an articulation surface of the tibial component to include an articulation feature whereby the articulation pathway of the femoral component is directed or guided by articulation feature.

Pathology of the human knee can arise from excessive and / or uneven loading of regions within the joint. Methods and apparatus are disclosed that enable displacement of soft tissue around the knee, without displacing or severing bone thereby altering the mechanical load distribution within the joint in a less invasive manner than previous techniques.

The invention relates to a device and method for assisting a subject to perform a motion such as a lift. The invention comprises a first anchor attachable to a first side of a joint of the subject's body, a second anchor attachable to a second side of the joint; and an elastic member connecting the first anchor and the second anchor, such that articulation of the joint in a first direction causes deformation of the elastic member and storing of energy, and articulation of the joint in a second direction causes relaxation of the elastic member wherein the energy is released and assists the subject to perform a motion in said second direction. The invention may be used at a subject's waist, ankle, wrist, knee, hip, elbow, shoulder, and / or at least one joint of the back and / or neck.

The invention reduces wear in total joint articulations by modifications of the shape of either component of the kinematic pair, so as to result in an annular surface contact between the two components. Fluid trapped between the two components within the inner contour of the annular contact area is pressurized under load due to elastic deformation of the components and exuded out through inter-articular gap over the surface of contact, aiding in lubrication and reducing the wear. Reduced to practice for a total hip joint with UHMWPE-metal pair, the wear rate tested in a hip joint simulator up to five million cycles was reduced by factor seven to fifteen compared to conventionally shaped components.

The invention relates to a prosthetic implant comprising a main body portion having a first surface for presentation to a receptive bone surface or into a bone cavity and a second surface for receipt of an articulating joint, and means on the implant adapted for attachment of a filamentary member, such as a cable. The invention also relates to a surgical tool for gripping the implant, comprising an elongate body having a first end surface for bearing on the prosthetic implant and means for attachment of the tool to the implant, directly or indirectly by means of the cable.

A device is provided including a distal nail portion and a proximal nail portion that can be connected to each other to attain a rigid configuration. The device is to be placed internally within the medullary cavities of at least two bones forming a joint to accomplish arthrodesis of the joint. The device is placed intramedullarily in order to minimize incision size, excessive bone resection and post-operative tendon damage and tenderness. Additionally, one particular method for using the device is provided that includes placing and affixing the distal nail in a bone of a joint, placing the proximal nail in another bone of a joint, connecting the distal nail to the proximal nail, doing the desired geometrical adjustments, affixing the proximal nail to the distal nail by tightening the connection and affixing the proximal nail to the other bone of the joint to attain a rigid configuration.

Embodiments of devices, apparatuses, kits, and methods for repairing and / or augmenting the articular surface and / or articular rim of a joint (e.g., repairing the anterior glenoid rim after an anterior shoulder dislocation).

A first articulating member for use with a second articulating member to form a prosthesis for use in joint arthroplasty for a joint formed between adjacent first and second bones in which a bone fragment having an exterior surface has separated from the first bone is provided. The first articulating member includes an articulating portion having an articulation surface for articulation with the second articulating member and an attaching portion connected to the articulating portion for attachment to the first bone. The first articulating member also includes a fragment portion connected to at least one of the articulating portion and the insertion portion. The fragment portion includes a surface for contact with the external periphery of the bone fragment.

A system for providing electrical stimulation of a joint. The system includes a wrap. The wrap includes a body, wherein the body is configured to be placed over the joint. The wrap also includes a first arm configured to be placed on a first side of the joint and attached to the body. The wrap further includes a second arm configured to be placed on a second side of the joint and attached to the body opposite the first arm. The wrap also includes a set of electrode locators. The set of electrode locators includes a first electrode locator, configured to receive a first electrode, a second electrode locator, configured to receive a second electrode, a third electrode locator, configured to receive a third electrode and a fourth electrode locator, configured to receive a fourth electrode.