Abstract: A method is provided for treating a spinal condition.

Abstract: A surgical procedure for implanting a graft according to which a dilator is inserted in a recipient opening and the graft is inserted in the dilator to cause outward expansion of the dilator into engagement with the portion of a bone surrounding the opening. After the dilator is removed from the opening, the bone surrounding the opening collapses around the graft to secure the graft in the opening.

Abstract: A method of treating a spinal condition includes placing disc replacement material in an intervertebral disc, thereby altering a loading characteristic of an adjacent vertebrae, and supporting the adjacent vertebrae by applying a bone filling material to either a superior or inferior vertebral body adjacent to the intervertebral disc. The disc placement material may also be configured to augment the intervertebral disc.

Abstract: A method of treating a spinal condition includes treating a degenerated disc with an interbody repair system, attaching bone anchors to posterior bone portions of the pair of vertebrae, and extending a posterior device between the bone anchors to prevent hyper-extension. The method further includes reinforcing a vertebral body with vertebral body treatment material and/or reinforcing an endplate of the vertebral body with an endplate treatment material.

Abstract: A prosthetic device and method of inserting same between adjacent vertebrae, according to which a first member of a relatively flexible material is adapted to extend between the vertebrae; and at least one second member of a relatively stiff material is supported by the first member.

Abstract: A vertebral implant and insertion tool for placing implants in the spine are disclosed. The implant has a tool engaging surface configured for intimate engagement with the insertion tool. The insertion tool configuration is particularly suited for being gripped at a plurality of angles. The insertion tool having a gripping end adapted for intimate engagement with an implant at a plurality of angles.

Abstract: An implant for placing in the spine is disclosed. The implant has a tool engaging surface on its trailing end configured for intimate engagement with an insertion tool. The insertion tool configuration is particularly suited for implants made of brittle materials including bone and bone substitutes. Also disclosed is an insertion tool having a gripping end adapted for intimate engagement with an implant. In one embodiment, the insertion tool is operable by axial movement of one gripping arm with respect to the other.

Abstract: Methods and devices for treating diseases and conditions that change the spacial relationship between the vertebral bodies and the intervertebral disks, or that cause instability of the vertebral column, or both, and a method and devices that allow the surgeon to access the intervertebral space to restore a more normal three-dimensional configuration of the space, with or without additionally fusing two adjacent vertebrae.

Abstract: An surgical apparatus and method are described for manipulating one or more osteochondral plugs, including, but not limited to, extracting and/or impacting the one or more osteochondral plugs.

Abstract: A prosthetic device for insertion into an intervertebral space may include a first articulating element formed of a ceramic material and a second articulating element configured to cooperate with the first articulating element to permit articulating motion. The second articulating element also may be formed of a ceramic material. A first polymer component may be joined to the first articulating element at a first ceramic-polymer interface and a second polymer component may be joined to the second articulating element at a second ceramic-polymer interface. A method of manufacturing the disc is also disclosed.

Abstract: Orthopedic compositions are provided that include a homogeneous mixture of a biocompatible polymer and a bioactive particulate ceramic wherein the ceramic has an average particle size of not more than 500 nm are provided. The compositions may be used to form bone cement or various spinal implants, including spinal spacers, interbody fusion cages, bone plates and bone screws. Methods for stabilizing a spine, for correcting a bone defect, and for promoting fusion of adjacent vertebrae are also provided.

Abstract: A surgical instrument tray shipping tote identification system is provided. During transit to or from a medical facility, processing center, distribution center or other location, multiple surgical instruments trays are placed in an instrument tray shipping tote. Each instrument tray includes at least one RFID transponder tag storing identification information about that tray. The shipping tote has a bar coded shipping label affixed to one surface generated at the point of origin. When the tote arrives at the distribution center, it is placed on a conveyor system that includes a reading station having an RFID transceiver and a bar code reader. Information read from the RFID transponder tags and the bar code label is transmitted by a controller to an external database to check for any off-nominal status indicators. Once this check is performed, an indication is sent back to the controller and an appropriate indicator on the identification system is activated.

Abstract: An intervertebral prosthetic device and method for spinal stabilization, according to which a prosthetic device is implanted relative to two vertebrae and is positioned so that it makes a rigid connection with one of the vertebra and a non-rigid connection with the other vertebra.

Abstract: Pedicle screws are secured in two columns, one along each side of the spine. Cross support rods have ends connected to pedicle screw heads. A longitudinally extending rod is supported on the cross supports and recessed in the cavity created by removal of portions of spinous processes, providing a reduced profile of the installed construct. Several types of cross supports are shown such as: arms from the screws inward to rings or yokes connecting the longitudinal rod; cross rods with ends connected to the screws and having centrally-located yokes for the longitudinal rod; cross rods with articulating longitudinal rod portions fixed or swiveled to them. These cross rods may have end portions angled posterior toward anterior to accommodate lateral positioned pedicle screws, but shorter cross rods without angled end portions enable medialized pedicle screw orientation.

Abstract: An RFID tag that is integrated into a substantially cylindrically-shaped structure that can be attached to an object to be identified through radio frequency identification techniques by sliding the substantially cylindrically-shaped structure over at least a portion of the object.

Abstract: A prosthetic device and a method of implanting same between two vertebrae of a vertebral column to stabilize the column, according to which each vertebrae is engaged by a spacer, and the spacers are connected to permit relative movement between the spacers so that the distance between the spacers can vary to conform with the distance between the vertebrae and accommodate bending movements of the vertebral column.

Abstract: A method for implanting a prosthetic spinal disc nucleus in an intervertebral disc nucleus space generally includes: (a) making a hole in the annulus of a disc, with the hole having an undilated size that is smaller than the cross-sectional size of a folded prosthetic disc nucleus; (b) using an implant instrument to dilate the hole in the disc annulus; (c) using the implant instrument to pass a straightened prosthetic disc nucleus through the dilated hole and into the disc nucleus space; (d) withdrawing the implant instrument and allowing the hole in the disc annulus to return to a size smaller that its dilated size; and (e) causing or allowing the prosthetic disc nucleus to assume a folded configuration with a cross-sectional size that is larger than its straightened size. A device for use in the method is also disclosed.

Abstract: A selective filtering collection and delivery system for collecting and delivering autogenous bone to and from a surgical site is provided. The selective filtering collection device includes a suction nozzle, suction nozzle assembly and a vacuum source. Disposed in parallel between the suction nozzle assembly and the vacuum source are a removable filter cartridge and a filter bypass tube. A switch on the suction nozzle assembly may be actuated to provide suction to the suction nozzle through either the bypass tube or through the filter cartridge. When suction is applied through the filter cartridge, autogenous bone is collected on a filter medium within the cartridge. Additionally, the cartridge may be removed and directly placed into a delivery device. The delivery device includes a ratchet system that actuates a plunger base to accurately extrude the bone material from the filter cartridge into the desired surgical location.

Abstract: Embodiments include selectively expandable composite structures useful as spinal arthroplasty devices such as intervertebral disc prostheses. The structures may comprise an outer shell comprised of a non-hydrogel polymer material. The structures also may comprise at least one core positioned within the outer shell. The core may be comprised of a hydrophilic polymer. The core may expand upon hydration, thereby deforming the outer shell. The selectively expandable composite structures may be implanted in a dehydrated form and then expand during re-hydration following implantation.

Abstract: The invention relates to a technique for precisely locating a line containing a predetermined point within the surgical site using a series of levels and plumb lines and internal anatomical features of the surgical site, using this location to precisely position and temporarily affix a site preparation scaffold relative to the patient's anatomy so that site preparation instruments can be introduced into the site at precise locations governed by the scaffold geometry and patient anatomy. This precise positioning of the scaffold also provides a way for the surgeon to use patient anatomical features to reliably and precisely prepare the surgical site. Scaffolds having angling features further increase the precise preparation of the surgical site. This increased precision in site preparation increases the probability of a successful procedure, and decreases the likelihood that additional surgery may be needed.