摘要:
Devices for implantation into an intervertebral disc can include a membrane support member to augment a disc having a defect. A defect in the anulus of a disc can be repaired using a prosthesis such as a barrier. The barrier can include a sealant and an enlarger. The barrier can be implanted into the disc using a delivery cannula, an advancer and at least one control filament to control the positioning of the barrier. A stiffening element can be included within the barrier to impart stiffness to the barrier. The support member can also be connected to an anchor.
摘要:
A vertebral disc prosthesis, a method of implanting a prosthesis and a deployment device is provided. The prosthesis may be implanted into the interior region of the vertebral disc so as to displace existing vertebral tissue, such as NP. The size or amount of the prosthesis inserted into the interior region of the vertebral disc may be a characteristic of the disc or the prosthesis. For example, the amount or size of prosthesis inserted into the disc may be dependent upon restoring the functionality of the disc (e.g., the ability of the disc to transfer nutrients or otherwise survive, the ability of the disc to carry the required loads and absorb stress or the reduction of pain). Restoring disc function may be determined by the resulting disc height desired, the resulting disc pressure desired or the resulting disc volume desired. The prosthesis may be sized or positioned within the interior of the vertebral disc such that it is spaced from at least one of the end plates of the vertebral disc. The prosthesis may be formed of a material having a compression strength that is less than 4 mn/m2. A deployment device may be used to facilitate placement of the prosthesis within the vertebral disc. The prosthesis may include a grouping of multiple components that can be deployed as group.
摘要:
The present invention provides methods and devices for treating the annulus of an intervertebral disc. The methods and devices can employ an expandable treatment device which is deployed at least partially in the subannular space. Fixation devices and methods are also disclosed, which help to secure the treatment device in place.
摘要:
A modular prosthesis that may be implanted in a highly minimally invasive manner. Specifically, the modular prosthesis may include a neck and an anchor. Both the neck and the anchor are configured to be inserted and connected together through a lateral aspect of a long bone adjacent to the proximal end of the long bone. In one exemplary embodiment, the neck includes a body having a head end, configured for attachment to another prosthetic component, such as a corresponding articulating component, and an aperture extending therethrough. The anchor may be sized for receipt within the aperture formed in the neck. Additionally, the anchor may be configured such that the anchor engages the walls forming the aperture in the neck to secure the components together.
摘要:
Systems for minimally invasive disc augmentation include an anulus augmentation implant suited for minimally invasive deployment. A nucleus augmentation component may be included. The anulus augmentation implant shields weakened regions of the anulus fibrosis and/or resists escape of natural nucleus pulposus and/or the nucleus augmentation component. Methods and deployment devices are also disclosed.
摘要:
A method for constantly controlling a direct application of pressure for bonding porous coatings to substrate materials used in orthopaedic implants. The direct pressure is applied to an interface between the porous coating and the substrate material via a pressure application mechanism unaffected by heat and air pressure conditions of the bonding process. The pressure application mechanism maintains a pressure on the implant which is constantly controlled throughout the bonding process.
摘要:
A prosthesis for implantation in a femur has a metallic stem portion having a smooth outer surface and a distal tip. A polymethylmethacrylate (PMMA) sleeve surrounds and is in contact with the stem portion. The sleeve has a cavity for receiving the stem tip and a bottom of said cavity spaced from the tip. A metal sheath has a cavity for receiving the sleeve. The metal sheath has a porous outer tissue ingrowth surface and a roughened inner surface. The PMMA sleeve is bonded to the inner surface of the metal sheath with a PMMA bone cement. The stem portion, sleeve and metal sheath all taper inwardly moving from a proximal stem portion to a distal stem portion.
摘要:
A prosthetic device includes a first component and a second component. The first component of the prosthetic device includes a polymer composite configured as an articular surface and having a wear rate of less than approximately 10−7 mm3/Nm. The polymer composite includes a first polymer and a second polymer. The first polymer comprises at least 10 weight percent of the polymer composite. The second component of the prosthetic device is configured to be implanted on a bone and includes a region of porosity that is customized for bone in-growth in a specific joint of a patient.
摘要:
Prosthetic hip stems and acetabular cups for use in prosthetic hip joints. The hip stem may include a core having a stem portion and a neck portion, a polymer matrix layer substantially covering the stem portion of the core, and a porous metal layer substantially covering the polymer matrix layer. The polymer matrix layer connects the core and the porous metal layer and provides a stiffness for the hip stem which more closely mimics the stiffness of bone than do known hip stems. The hip stems and acetabular cups additionally include a number of improvements adapted for more optimized results with certain types of patient anatomy, such as the anatomy of female patients, for example.
摘要:
The invention solves the problem of anchoring a prosthetic component into compliant, cancellous bone by a thin, preferably pure titanium, or a titanium-based alloy, perforated, hence hydraulically open, shell (1, 13), spaced apart from the second, non-perforated shell (2, 14). In most applications, dictated by the anatomical site of insertion, shells are approximately hemispherical in form, connected to each other at the equator The solid shell may contain a further, articulating component of the joint, e.g. a polymer or a ceramic insert, or it may serve that function itself. One or both components of a joint prosthesis can be anchored according to the invention.