摘要:
Flexible cartilage-replacing implants are disclosed that use either or both of (1) enlarged peripheral rim components, and/or (2) elongated flexible reinforcing members that are embedded around the peripheral edge of an implant device. These types of anchoring devices, especially when used in combination, can provide flexible implants that can be implanted arthroscopically into synovial joints, for complete replacement of damaged cartilage segments.
摘要:
A buffer (10) for placement in a human knee between the femur and tibia comprises an outer sack (14) formed of a pliable material and having a one-way valve (22), a generally circularly shaped inner ring (16) received within the outer sack (14), and a friction reducing fluid (18) received within the outer sack (14) via the one-way valve (22). The inner ring (16) includes top and bottom surfaces (38,40) angled inwardly with respect to each other, such that the ring (16) is generally concave. The buffer (10) is configured for insertion between the femur and tibia so as to at least partially prevent the bones from contacting each other, which reduces the pain and discomfort associated with a loss of articular cartilage (12). The buffer (10) is arthroscopically inserted in the knee using an especially designed sleeve (20) configured for support of the buffer (10) during insertion.
摘要:
The invention comprises a combination of biological elements that will naturally remodel in vivo based on applied mechanical forces. The final composition will possess mechanical properties similar to cartilage or a disc, and significantly less stiff than bone or implants comprised of metals or plastics. The equilibrium stress conduction will minimize unnatural forces on neighboring healthy discs.
摘要:
Knotless suture anchors are disclosed for surgical use, which contain one or more types of ratcheting mechanisms that will allow a surgeon to pull a suture strand through an anchor device in one direction, without allowing the suture strand to travel or creep backward, in the other direction. This will allow a surgeon to emplace a number of such anchors in hard bone(s) or soft tissue(s), during installation of an implant device, while the various suture strands remain loose and do not interfere with proper positioning of the implant. When the implant device is roughly in position, the surgeon can gently “snug” all of the suture strands (which preferably should be braided, to provide a non-smooth surface that will enable a stronger and more secure grip by the ratcheting mechanism), so that they will all reach a moderate plateau of gentle yet firm tension. After the surgeon has ensured that the implant is in proper position, with all of the anchoring sutures in a “snug” status, a series of final tightening and tensioning steps can be carried out on all of the suture strands.
摘要:
Knotless suture anchors are disclosed for surgical use, which contain one or more types of ratcheting mechanisms that will allow a surgeon to pull a suture strand through an anchor device in one direction, without allowing the suture strand to travel or creep backward, in the other direction. This will allow a surgeon to emplace a number of such anchors in hard bone(s) or soft tissue(s), during installation of an implant device, while the various suture strands remain loose and do not interfere with proper positioning of the implant. When the implant device is roughly in position, the surgeon can gently “snug” all of the suture strands (which preferably should be braided, to provide a non-smooth surface that will enable a stronger and more secure grip by the ratcheting mechanism), so that they will all reach a moderate plateau of gentle yet firm tension. After the surgeon has ensured that the implant is in proper position, with all of the anchoring sutures in a “snug” status, a series of final tightening and tensioning steps can be carried out on all of the suture strands.
摘要:
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.
摘要:
A method provides a void creation device including an expandable structure adapted to undergo expansion in the cancellous bone volume of a bone selected for treatment. The expandable structure has at least one dimension so that the expandable structure will assume a predetermined shape and size when substantially expanded that compacts only a first volume of the cancellous bone volume to form a void, leaving a second volume of the cancellous bone volume substantially uncompacted by the expandable structure. A filling material is placed within the void through the percutaneous access path.
摘要:
Non-articulating semi-rigid spinal implants include upper and lower rigid endplates that define at least one aligned pair of rigid male and female members. The respective female member having an interior facing cavity and the respective male member facing toward the female cavity. At least one elastic member resides in each female member cavity. The device can include an optional housing with at least one bore for each of the at least one aligned pairs of female and male members. The housing bore is sized and configured to snugly encase each respective aligned pair of endplate male and female members while leaving an upper outer surface of the upper endplate and a lower outer surface of the lower endplate exposed.
摘要:
An artificial intervertebral disk, insertable between two adjacent vertebral bodies of a patient and joining the two adjacent vertebral bodies an articulated manner, includes an intermediate element embodied as an elastic ring and is inserted into one respective molded portion of two outer elements configured as metal plates. The outer elements are joined to the bones of the vertebral bodies via anchoring pins, especially titanium anchorings previously known in hip endoprosthetics. The radius of the concave molded portion is greater than the diameter of a circular cross-sectional area of the intermediate element such that compression of the intermediate element caused particularly by the patient's movement allows for a defined deformation.
摘要:
Devices and methods compress cancellous bone. In one arrangement, the devices and methods make use of an expandable body that includes an internal restraint coupled to the body. The internal restraint directs expansion of the body. In one arrangement, a method for treating bone inserts the device having the internal restraint inside bone and causes directed expansion of the body in cancellous bone. Cancellous bone is compacted by the directed expansion.