Abstract: A method for locking an elongate rod within a head of a bone anchor implant assembly that is configured for surgical implantation into a bone of a patient. The method includes providing an elongate rod, providing a separate shank and the head, and providing a closure mechanism configured as a one-part closure or two-part closure. The method further includes receiving the elongate rod in the channel and closing the channel with the closure mechanism. The one-part closure and two-part closure are configured to be interchangeable with each other for closing a channel of the head and locking the assembly and the elongate rod between arms of the head with the closure mechanism.

Abstract: A revision connector is configured to couple a new spine fixation rod to a previously implanted spine fixation rod that is secured to a plurality of vertebrae. The new spine fixation rod can be implanted and secured to vertebrae that are caudal and/or cranial with respect to the previously secured vertebrae.

Abstract: Orthopedic fixation devices, assemblies, and methods. The orthopedic fixation devices may comprise coupling elements, hook components, and/or bone fasteners. The bone fastener may be loaded into the coupling element through the bottom of a bore in the coupling element. The orthopedic fixation devices may include modular locking clamp assemblies that can be fixed onto fasteners that are already implanted in bone. The modular locking clamp assemblies can include polyaxial locking clamp assemblies, as well as monoaxial locking clamp assemblies. The hook components may include a female hook component slidably coupled to a male hook component.

Abstract: Various embodiments of craniofacial implants, surgical instruments, and techniques are described to provide improved surgical results.

Abstract: Various embodiments of craniofacial implants, surgical instruments, and techniques are described to provide improved surgical results.

Abstract: Orthopedic fixation devices, assemblies, and methods. The orthopedic fixation devices may comprise coupling elements, hook components, and/or bone fasteners. The bone fastener may be loaded into the coupling element through the bottom of a bore in the coupling element. The orthopedic fixation devices may include modular locking clamp assemblies that can be fixed onto fasteners that are already implanted in bone. The modular locking clamp assemblies can include polyaxial locking clamp assemblies, as well as monoaxial locking clamp assemblies. The hook components may include a female hook component slidably coupled to a male hook component.

Abstract: A medical apparatus including a bar with a first attachment loop, a second attachment and a plurality of hooks, wherein the medical apparatus is an arch bar.

Abstract: A sternal closure clamp device assembly for securing and retaining longitudinally divided halves of a sternum, the assembly having at least two sternal clamps retained by clamp receiving members, the clamp receiving members being joined by a linking assembly whereby the distance between the clamps can be adjusted and fixed.

Abstract: A sternal closure clamp device for securing and retaining longitudinally divided halves of a sternum, and its method of use, the device having a pair of body members each having engagement members adapted to abut the sides of the sternal halves, and at least one rib extension member having rib retaining members and attached to at least one of said body members, such that the rib extension member can be secured to a rib to reduce the force being applied directly to the sternal halves.

Abstract: An occipital clamping hook assembly includes a hook for engaging a first side of an occipital bone and a compressor movable relative to the hook for applying a compressive force to the occipital bone from a second side of the occipital bone. The occipital clamping assembly further includes a rod-receiving portion coupled to the hook for coupling a rod to the occipital bone engaged by the hook.

Abstract: An implant is described having a shaft (1) and a holding element (3; 30) connected therewith for connecting with a rod (100). A recess is provided in the holding element. The recess has a U-shaped cross section for accommodation of the rod and two free legs (7, 8; 32, 33) at one end which include an inner thread (9; 34). A closure element (20; 36) fixes the rod inserted into the U-shaped recess. The closure element has an outer thread cooperating with the inner thread of the legs. An abutment is provided at or in the holding element (3; 30) to limit tilting of the closure element about the rod at the time of final tightening of the closure element in the holding element. As a result thereof it is possible to keep the wall thickness of the receiver member small in spite of the large forces acting at the time of final tightening. The invention is applicable to both monoaxial screws and polyaxial screws as well as bone hooks.

Abstract: A polyaxial bone anchor has a locking element shaped and configured to allow an anchoring member (e.g., a screw or hook) to polyaxially rotate at large angles about a central axis of the bone anchor before compression locking the anchoring member within an anchor head.

Abstract: A connector for a spinal alignment system includes a base, a hook, a guide aperture, and a locking portion. The base includes a channel extending therethrough to receive a fixation rod. The hook extends from the base. The guide aperture is adapted to receive a bone fastener and the locking portion is adapted to engage the bone fastener. The guide aperture extends through one of the base and the hook and the locking portion is located in the other of the base and the hook. The locking portion is coaxial with the guide aperture such that the guide aperture guides a shaft of the bone fastener into alignment with the locking portion when the bone fastener is received by the guide aperture. The bone fastener cooperates with the base and hook to form a tension band construct that resists opposing forces acting on the construct. A rod locking fastener engages the channel and the fixation rod to secure the fixation rod in the channel.

Abstract: A mechanism for fixing a spinal support to vertebrae includes a support member and a pedicle screw component. The support member comprises an elongated end comprising a longitudinal axis. A hook connects to the elongated end and receives the vertebrae. The hook is angled in three different planes with respect to the longitudinal axis. A connector section connects the elongated end to the hook and is angled with respect to the elongated end and comprises a thickness less than a thickness of the elongated end. The pedicle screw component comprises a fixation component anchored in the vertebrae. The fixation component comprises a socket; a screw head comprising a bulbous end that fits into the socket; and a channel that receives the elongated end. A pin causes outward expansion of the bulbous end; and a blocking mechanism is attached to the screw head and adjacent to the elongated end.

Abstract: An improve spinal surgical implant used primarily in the posterior aspect of the spinal column for spinal reconstruction; revision surgery; deformity correction; and/or tumor surgery and/or trauma surgery of the cervical, thoracic and/or and lumbo-sacral spine.

Abstract: A headless polyaxial screw system comprises a longitudinal member comprising an outwardly protruding and expandable round bulbous body, a fixation component directly connected to the bulbous body, where the fixation component receives the bulbous body, and a pin engaged within the longitudinal member via a first channel bored through the longitudinal member and contacting the bulbous body causing the bulbous body to outwardly expand.

Abstract: The present invention relates to a process for producing components consisting of magnesium or magnesium alloy by sintering. This process makes it possible, for the first time, to produce components consisting of magnesium or magnesium alloy which provide outstanding elasticity together with a sufficient strength. Materials of this type can be used as biocompatible endosseous implant materials.

Abstract: The present invention relates to a fixation device for a correction bar used in the operation of pectus excavatum, and more particularly, to a fixation device for securing the correction bar inserted into a thoracic cavity to a rib in an operation of correcting pectus excavatum, which a sort of thoracic malformation. The fixation device of a correction bar used in the operation of pectus excavatum includes a plurality of rib fixation units fastened to the correction bar and each having a rib support portion and a fastening portion formed at both ends thereof, the rib support portion being formed of a hook portion bent in such a manner as to be hooked and secured to a rib, and the fastening portion being formed of a rectangular through-hole or a slot; and a fastening screw unit adapted to fasten the plurality of rib fixation units hooked and secured to upper and lower ribs to the correction bar through the respective fastening portions of the plurality of rib fixation units.

Abstract: In one embodiment of the present invention a system for connecting a fastener element (e.g., a pedicle screw) relative to a rod for the purposes of vertebral fixation is provided. The system may permit multi-axial movement between the fastener element and the rod. Further, the system may permit the angular relationship between the fastener element and the rod to be held in a desired orientation. For the purposes of describing and claiming the present invention, the term “rod” is intended to refer to any elongated structure. Such an elongated structure may be solid or hollow and may have any desired cross-section (e.g., circular, oval, square, rectangular). Further, for the purposes of describing and claiming the present invention, the term “interference fit” is intended to refer to physical contact between two or more components.

Abstract: A cervical intra-laminar fusion implant to be placed in cervical lamina includes a first lateral surface including a first arched edge, a second lateral surface positioned opposite to the first lateral surface, the second lateral surface including a plurality of posterior windows and a second arched edge, a top wall attached to the first lateral surface and the second lateral surface, the top wall having a plurality of teeth, a bottom wall positioned opposite to the top wall and attached to the first lateral surface and the second lateral surface, the bottom wall having a plurality of bottom teeth, a plurality of internal voids configured through the top wall and the bottom wall, and a connection mechanism connected to the top wall. The connection mechanism is positioned superior over the cervical lamina.

Abstract: A targeting surgical instrument for use in spinal disc replacement includes a first arm, a second arm and a body portion. The first arm is configured to be longitudinally aligned with a mid-line of a spine and to be at least partially received on an endplate of a lower vertebra of spinal cavity. The spinal cavity is defined by a lower vertebra and an upper vertebra of the spinal cavity. The second arm is positioned at an angle relative to the first arm. The second arm defines an insertion angle for a spinal implant. The body portion connects the first arm and the second arm. The body portion includes a plurality of radial opaque markers located to allow alignment of the first arm on the mid-line of the spine.

Abstract: Locking mechanism for a broken or fractured bone, comprising a medulla nail with a proximal portion which may incorporate perforations and a distal portion, and at least one locking aid, characterised in that the distal portion has a surface structure which is designed so that the bone can be stabilised by means of the medulla nail due to the at least one locking aid acting on the surface structure of the nail through the bone from outside, preferably preventing it from rotating and/or being subjected to axial stress.

Abstract: A medical apparatus for alleviating the symptoms associated with spinal stenosis have a body including first and second supports disposed along the length of the body. The first support is configured to accommodate at least a portion of a vertebral component of a first vertebra disposed above or below a second vertebra. The second support is configured to accommodate at least a portion of a vertebral component of the second vertebra. The distance between the supports is sufficient to increase the space between the first vertebra and the second vertebra. Methods for using the apparatus include implanting the apparatus into a subject.

Abstract: Disclosed are devices and systems for spinal fixation and dynamic stabilization. Elongated members may be positioned lateral to spinous processes and coupled to two or more vertebrae. Interspinous members may be positioned between adjacent spinous processes and coupled to the elongated members. One embodiment of an interspinous member comprises a body and two lateral portions. The lateral portions may couple to the elongated members to position the interspinous members. An interspinous member and the positioning of the interspinous member may allow selected movement between the adjacent spinous processes.

Abstract: A force diffusion hook includes a hook element and a connecting member receiving portion for receiving a connecting member to stabilize a spinal column segment. The hook element defines a receptacle for receiving a bony portion. A force diffusion member extends along the receptacle between the hook element and the bony portion. The force diffusion member is deformable to distribute load between the bony portion and the hook element.

Abstract: A bone fixation device includes a rod including a first portion extending from a proximal side of the rod, and a second portion extending from the first portion, wherein the rod is inserted into a medullary canal of an ulna bone, the first portion includes a plurality of longitudinally displaced screw holes, having axes whereby at least two screws inserted into the screw boles extend in discrete directions into a metaphyseal portion of the ulna. The bone fixation device also includes a curved extension portion extending from the proximal side of the rod to capture an olecranon of the ulna. The device provides the benefits of an intramedullary nail and proximal tension band type fixation in a single device. The fixation device permits a minimally invasive treatment of proximal ulna fractures that may otherwise be under treated.