705 results about "Vertebral bone" patented technology

Stent systems and methods for expanding and deploying stents in hard tissue such as bone, more particularly within a vertebral body. One exemplary method includes using a stent body that is coupled to a high speed rotational motor with the stent expandable and detachable from an introducer working end. In one embodiment, the stent is a deformable metal body with zig-zag type struts in an expanded configuration that carries diamond cutting particles bonded to the strut surfaces. The “spin” stent is rotated at high rpm's to remove cancellous bone from the deployment site together with irrigation and aspiration at the end of the probe that carries the stent. The stent may be expanded asymmetrically, such as with first and second balloons or by using an interior restraint, to apply vertical distraction forces to move apart the cortical endplates and support the vertebra in the distracted condition. The cancellous bone about the expanded stent as well as the interior of the stent can be filled with a bone cement, allograft or other bone graft material. In one method of use, the spin stent is designed and adapted for (i) treating a vertebral compression fracture (VCF) or for (ii) reinforcing an osteoporotic vertebral body.

A method and system for marking and guiding the insertion of securing members (e.g., pedicle screws) of a spinal fixation device. In one embodiment, the marking and guidance method and system includes the use of a guide tube configured to be inserted into a patient's back until a first end reaches an entry point on or near a vertebral bone of the patient's spinal column, wherein the guide tube includes a hollow cylindrical channel along its longitudinal center axis; a penetrating device configured to be positioned within the cylindrical channel of the guide tube and having a sharp tip configured to protrude outwardly from the first end of the guide tube so as to allow the first end of the guide tube to penetrate through the patient's back muscle and tissue and reach the vertebral bone at the entry point; a marking pin configured to be inserted through the cylindrical channel of the guide tube, after removal of the penetrating device, until a first end of the marking pin having a sharp tip reaches the entry point; and a pushing device configured to be inserted through the cylindrical channel of the guide tube and provide a driving force at a second end of the marking pin, opposite the first end, so as to drive and secure the first end of the marking pin into the vertebral bone, wherein the marking pin identifies the location of the entry point on the vertebral bone for subsequent implantation of a securing member of a spinal fixation device.

The present invention is directed to a device that can be placed between two adjacent vertebrae, and that is used to repair an injury or defect in the anulus of the intervertebral disk. The implant is characterized by having a flexible structure anchored to the vertebral bone, the flexible structure connected with a patch held in place over the injury or defect. The flexible structure has a hollow interior space which can sustain inside it a hydrogel cushion. The hydrogel cushion acts as a shock absorber for the spine, maintains height of the intervertebral disk space, and prevents further disk herniation due to the narrowing of the intervertebral disk space.

Devices and methods are provided for treating a bone structure (such as, e.g., reducing a bone fracture, e.g., a vertebral compression fracture, or stabilizing adjacent bone structure, e.g., vertebrae) is provided. The device comprises rigid or semi-rigid members, each of which comprises a common base and a plurality of ribs that extent along the a longitudinal portion of the common base. The device is configured to be placed in a collapsed state by engaging the pluralities of ribs of the members in an interposed arrangement, and configured to be placed in a deployed state by disengaging the pluralities of ribs. The ribs can be any shape, e.g., flutes, that allows opposing ribs to intermesh with one another. In this manner, the device has a relatively small profile when placed in the collapsed state, so that it can be introduced through small openings within the bone structure, while preserving the shear strength of the members during deployment of the device.

A method and a distracter for replacing a removed, intervertebral disc with a prosthesis. An inter-body distracter is inserted within the intervertebral space between adjacent vertebrae, the vertebrae are distracted and are supported by the distracter. A fluid, curable polymer is injected into the intervertebral space and around the distracter and then the polymer is cured to a semi-rigid, pliable, elastically deformable state. The distracter is then disabled from supporting compressive forces applied by the vertebrae and remains in place. The preferred distracter is a scissors jack having intermediate bearings joined by links to support feet. One of the bearings has a threaded lateral bore and the second bearing has a lateral bore. A rod extends through the bores and has a threaded portion extending from a first end of the rod and threadedly engaging the threaded bearing. The inside diameter of the second bore is greater than the outside diameter of the threaded portion of the rod so the rod is axially slidable through the second bore. A thrust bearing is fixed on the threaded rod and positioned laterally outwardly of the second bearing for forcing the second bearing laterally toward the first bearing upon rotation of the rod in one direction and for permitting the rod to be withdrawn from the bearing by rotating the rod in the opposite direction and disengaging it from the first bearing. Alternative distracters are also disclosed.

The invention provides an intervertebral disk prosthesis. The prosthesis comprises: a first fixing element having both an anchoring first face for anchoring in one of the vertebrae and a co-operation second face; a second fixing element having both an anchoring first face for anchoring in the other vertebrae and a co-operation second face; a first prosthesis element having both an active first face and a co-operation second face, said co-operation faces of the first fixing element and of the first prosthesis element serving to fasten the two elements together; a second prosthesis element having both an active first face and a co-operation second face, said co-operation faces of the second fixing element and of the second prosthesis element serving to fasten the two elements together; and each of said active faces of the prosthesis elements defining at least a portion of a spherical cap that is respectively concave or convex.

The invention relates to an assembly for treating degeneration of a damaged intervertebral disk disposed between two vertebrae. The treatment assembly includes cells that may be analogous to those of the intervertebral disk, and that are suitable for implanting in said disk; and an intervertebral implant. The intervertebral implant includes an intervertebral spacer for placing between said vertebrae, and a fastener device for fastening said spacer on said vertebrae.

An orthopedic implant comprising a deformable, expandable implant body configured for treating abnormalities in bones, such as compression fractures of vertebra, necrosis of femurs and the like. An exemplary implant body comprises a small cross-section threaded element that is introduced into a bone region and thereafter is expanded into a larger cross-section, monolithic assembly to provide a bone support. In one embodiment, the implant body is at least partly fabricated of a magnesium alloy that is biodegradable to allow for later tissue ingrowth.

An orthopedic device for implanting between adjacent vertebrae comprising: an arcuate balloon and a hardenable material within said balloon.

In some embodiments, the balloon has a footprint that substantially corresponds to a perimeter of a vertebral endplate. An inflatable device is inserted through a cannula into an intervertebral space and oriented so that, upon expansion, a natural angle between vertebrae will be at least partially restored. At least one component selected from the group consisting of a load-bearing component and an osteobiologic component is directed into the inflatable device through a fluid communication means.

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 apparatus for stabilizing and promoting fusion between adjacent vertebrae includes at least a pair of implants to promote bone growth and to fuse with vertebral bone. The implants are joined by a connector. Preferably the implants are inserted into receiving bores in a non-parallel configuration and/or the connector joins the implants so as to bias the implants to a non-parallel configuration. A pair of connecting members also preferably secure the implants to each of the adjacent vertebrae. A method of using the apparatus provides for stabilizing between vertebrae where the original cushioning disc has deteriorated or become damaged. The implants are connected together. Also in the method, the implant receiving bores are non-parallel and/or the implants are biased to non-parallel configurations by joining the implants to the connecting element so as to reduce the inadvertent disturbance of the implants from the receiving bores and to further stabilize the implants overall during the fusion process.