Abstract: Disclosed is an apparatus for forming an arcuate channel in one or more segments of a bone, bony structure or adjacent vertebrae of a spine. The apparatus includes, inter alia, a base member which is positioned proximate to the surgical site, a support arm extending proximally from the base member, an arcuate guide member and a drill assembly. The arcuate guide member is slidably mounted to the support arm. The drill assembly is operatively coupled to the support arm and includes a drill bit attached to the distal end of a flexible drive cable. The flexible drive cable extends axially along the support arm and is axially and rotationally movable with respect thereto. The drill bit is operatively coupled to an end of the arcuate guide member such that when the drill assembly is moved distally, the arcuate guide member slides with respect to the support arm and forces the drill bit to traverse an arcuate path.

Abstract: Devices and methods are provided for positioning and forming bone tunnels. In one embodiment, a surgical drill guide apparatus is provided. The apparatus can include a first guide member having a longitudinal passageway extending therethrough for aiming a first guide pin along a first path to form a first bone tunnel. The apparatus can also include a second guide member having a longitudinal passageway extending therethrough for aiming a second guide pin along a second path to form a second bone tunnel. The first and second guide members can extend at an angle relative to one another and they can be offset such that axes of the guide members do not intersect.

Abstract: Intramedullary osteosynthesis device is capable of adopting a profiled H-shape in a closed introductory state in order to be easily implantable and an X-shape in an open implanted state for good fixation in the bone.

Abstract: The invention relates to a preparation device for preparing an intervertebral disc compartment (14) which is delimited by a first and a second vertebra (16, 18). Such a preparation is carried out prior to the insertion of an intervertebral disc prosthesis (110), in order to guarantee a correct positioning of the intervertebral disc prosthesis between the vertebrae (16, 18). The preparation device (10) comprises a reference frame (22), which is capable of being fastened above an operating table (12), and a first fixing element (58) which is capable of being rigidly connected to the first vertebra (16) are capable of being fastened to the reference frame (22) in varying first positions. A second fixing element (68) is capable of being rigidly connected to the second vertebra (18) and capable of being fastened to the reference frame (22) in varying second positions. A material-abrading tool (78) is capable of being fastened to the reference frame (22), preferably in varying positions.

Abstract: The described devices are bound spinal implants that may be surgically implanted into the spine to replace damaged or diseased discs using a posterior approach. The discs are prosthetic devices that approach or mimic the physiological motion and reaction of the natural disc.

Abstract: An intervertebral space distraction and implantable device assembly provides sequentially axially wider spacers that are to be sequentially inserted into and removed from an intervertebral space to widen the space until a desired anatomical spacing of the adjacent vertebral bones is restored. The set of spacers includes a porous spacer that is as wide as the spacer that restores the desired anatomical spacing. The porous spacer can therefore be left implanted in the intervertebral space to promote fusion of the adjacent vertebral bones.

Abstract: A tissue removal device and method of using the device to remove tissue from a patient is provided. The tissue removal device comprises a tissue removal probe and a sheath slidable relative to the probe. The probe has a tissue removal element, and the sheath has a portion that exposes the tissue removal element. The sheath distal end may be pre-shaped to bend when slid distal to the probe. The probe may have a window through which the tissue removal element is exposed.

Abstract: An instrument for handling a joint component of a joint prosthesis, which joint component includes a joint surface, includes a grip portion, a suction element in the form of a suction cup with an air-vent opening, the suction cup being placeable in a sealing manner against the joint surface, and a pressure-relief valve associated with the air-vent opening of the suction cup. The pressure-relief valve is coupled to an actuating element which is arranged so as to be movable in the region of the grip surface of the grip portion and, when gripped with one hand, is actuatable with a finger or the thumb of that hand, so that on actuation of the actuating element the valve is lifted away from the air-vent opening.

Abstract: A substantially rigid plate is secured to a medial portion of a clavicle relative to a fracture in the clavicle. The plate is positioned so that it extends at least partially over a distal portion of the clavicle relative to the fracture. The plate has surfaces that define a first opening through which a suture can pass. A hole is formed in the clavicle. A washer may be positioned at a side of the plate opposite the clavicle. Alternatively, the plate may include suture holes or edge features for securing a suture. A suture is secured to the washer, to at least one suture hole or to at least one edge feature, and extends through the first opening, through the hole in the clavicle and is secured to the coracoid process.

Abstract: The present invention relates to an intramedullary nail distal targeting device (20) adapted to be installed to an external jig system (A) having a proximal attachment (B) to support an intramedullary nail (C) thereon and an extension arm (D) secured to the proximal attachment (B), the nail distal targeting device including a drill guide (21) being defined by an abbreviated cylindrical body (23) having at least a pair of guide slots (24, 24?) each of the guide slots (24, 24?) having a scalloped inner surface (25), an attaching mechanism (22) being provided at the upper portion of the drill guide (21), the attaching mechanism (22) secured in a rotating and sliding manner to a distal end of the extension arm (D) and at least a pair of guide sleeves (10, 10?) being telescopically fitted correspondingly into the slots (24, 24?) of the drill guide (21), each of the guide sleeves (10, 10?) having a scalloped outer surface to correspondingly fit into the guide slots (24, 24?), each of the guide sleeves (10, 10?) bei

Abstract: A growth control device includes a bone plate having a stepped profile defined by a first level, a second level and an intermediate ramp connecting the first and second levels. The first level includes a first threaded hole for receiving a first bone fastener and the second level includes a second threaded hole for receiving a second bone fastener. The bone plate includes a proximal pair of side female notches, a distal pair of side female notches, a proximal guide hole and a distal guide hole.

Abstract: There is provided a method and system for determining a distal cut thickness and posterior cut thickness for a femur in a knee replacement operation, the method comprising: performing a tibial cut on a tibia; performing soft tissue balancing based on a desired limb alignment; measuring an extension gap between the femur and said tibial cut while in extension; measuring a flexion gap between the femur and the tibial cut while in flexion; calculating a distal cut thickness and a posterior cut thickness for the femur using the extension gap and the flexion gap and taking into account a distal thickness and posterior thickness of a femoral implant; and performing said femoral cut according to the distal cut thickness and posterior cut thickness.

Abstract: An endoprosthesis component is formed from a ceramic material and in which the ceramic material is partially coated with a titanium alloy. An uncoated surface portion of the endoprosthesis component is designed to interact as slide surface with another endoprosthesis component. A coated surface portion of the endoprosthesis component is designed to establish a connection to a bone. The part of the ceramic material forming an interface to the coating has a roughness Ra of between 2.5 ?M and 7 ?M, creating a firm connection between the coating and the ceramic material. The invention further relates to a method for producing such an endoprosthesis component. To achieve the desired roughness of the surface, the ceramic component is presintered at a temperature of between 880° C. and 980° C. and is then treated with a blasting material.

Abstract: An implant has a first contact surface to contact a first vertebral body endplate and a second contact surface to contact a second vertebral body endplate adjacent the first vertebral body. The implant is deployable, when positioned within an intradiscal space between the first and second vertebral bodies, from a first non-expanded condition where the first contact surface has a first effective footprint area A1 to a second expanded condition where the first contact surface has a second effective footprint area A2. The ratio A2/A1 is at least 1.05.

Abstract: Methods, systems, devices and tools for placing bone stabilization components in a patient are provided. The systems and devices have a reduced number of discrete components that allow placement through small incisions and tubes. More particularly, the present invention is directed to systems and methods of treating the spine, which eliminate pain and enable spinal motion, which effectively mimics that of a normally functioning spine. Methods are also provided for stabilizing the spine and for implanting the subject systems.

Abstract: The retractor system for use in spinal surgery and other types of surgical procedures that is a simple and efficient solution for minimally invasive access to thoracolumbar spine is disclosed. The fully customizable design allows the surgeon to independently angle the retractor blades and expand the retractor in both cephalad-caudal and medial-lateral directions. With an offering of a range of blade lengths, access can be tailored to the patient's anatomy. Auxiliary instruments such as the retractor inserter, universal hex driver and blade removal instrument allow quick and controlled access to the surgical site. The retractor system provides versatility and control ensuring minimal tissue trauma.

Abstract: A surgical procedure is disclosed utilizing a cordless surgical handpiece powered from a sterile battery pack that contains a battery in condition for immediate use without further charging or sterilization. The battery chemistry is based upon lithium/manganese dioxide, and the battery after a single use may be disposed of into non-hazardous waste. The compact surgical handpiece has a brushless DC motor and a manually operated external trigger for activating and controlling the motor operations. Interengaging sets of contacts on the handpiece and battery are adapted to become lockingly and conductively interengaged upon rotation of the battery pack relative to the handpiece, in a manner that rapidly achieves correct alignment of the parts and also ensures stable mechanical attachment and support during the surgical procedure.

Abstract: The present invention relates to one or more tibial spacer blocks used during knee arthroplasty, each configured to be temporarily positioned upon a resected proximal portion of a tibia (essentially mimicking the tibial component of the knee prosthesis), for performing a range of motion analysis and for checking flexion and extension gaps prior to cutting the distal or posterior femur. Preferably, the spacer blocks each include an attachment arrangement configured and arranged to mate with a complementary attachment arrangement of an alignment tower and/or a femoral cutting guide. The alignment tower, which is configured to be used with an alignment rod, is used for verifying the alignment of the limb's mechanical axis when the spacer block is positioned between the tibia and the femur. The femoral cutting guide is used for guiding a cutting member into proper orientation for resecting a distal or posterior portion of a femur.

Abstract: A compression plate kit that allows for manual compression of a bone discontinuity includes a bone plate, two or more reduction screws, and a compression clamp. The compression clamp can include engagement members configured to engage the reduction screws, thereby allowing a practitioner to compress a bone discontinuity by manually closing the compression clamp. One or more implementations of a kit of the present invention can provide a practitioner with physical or tactile feedback during the compression of a bone discontinuity, and thus, provide the practitioner with the ability to better control the compression and spacing of bone portions during a reduction.

Abstract: A flexible piece of barrier material for use in preventing or minimizing adhesions and fibrous attachments following anterior lumbar surgery. In one embodiment, the barrier structure comprises a multiple level device shaped as a generally wider tongue to function as a barrier at or above the L4-5 level, and a generally narrower lower section to function as a barrier at or below the L5-S1 level. The structure also can include a recessed waist section along an edge opposite the tongue to allow for easier placement in the L4-5 area. In another embodiment, a single level barrier for use at or above L4-5 is shaped as a tongue with a tapered outer extension to allow the barrier to extend laterally onto the psoas muscle to provide for identification of the barrier upon reoperation.