A device for hydrating particulate bone material is provided. The device comprises a tubular member having an interior surface and an exterior surface. The interior surface is configured to receive the particulate bone material and a hydration fluid. The exterior surface has a plurality of pores configured to allow the hydration fluid to flow into the interior surface of the tubular member and hydrate the particulate bone material. The plurality of pores are smaller in size than the particulate bone material. Methods of dispensing particulate the bone material are also provided.

Disclosed herein are a bone plating system and a method for utilizing the same. The bone plating system may include first and second bone plates in contact with respective first and second bones, a cross-connector, a cutting guide and a targeter device. The cross-connector may have a first end and an opposite second extending along a longitudinal axis from the first bone plate to the second bone plate. The cutting guide may have an elongate body placed on one of the first or second bones. The targeter device may have a drill guide to align the cross-connector with the first and second bone plates. A method for fixing the bone plating system to the first and second bone may include using the targeter device.

A device for hydrating particulate bone material is provided. The device comprises a tubular member having an interior surface and an exterior surface. The interior surface is configured to receive the particulate bone material and a hydration fluid. The exterior surface has a plurality of pores configured to allow the hydration fluid to flow into the interior surface of the tubular member and hydrate the particulate bone material. The plurality of pores are smaller in size than the particulate bone material. Methods of dispensing particulate the bone material are also provided.

Devices and methods for mixing and preparing therapeutic pellets are described. In one aspect, the present disclosure may include a medical device for mixing and preparing pharmaceuticals. The medical device may include a body sized and shaped to be supported by a human hand. The body may be elastically flexible between a relaxed shape and a flexed shape. In the relaxed shape, the body may form a basin and may be shaped and sized to receive a vessel for mixing or forming the therapeutic pellets. In the flexed shape, the bowl may be configured for controlled pouring of the therapeutic pellets.

A system for use in stimulating bone growth, tissue healing, and/or pain control is described. The system includes a screw, a battery, a controller, and means for connecting the battery such that current is routed from the battery through the screw and thence to a target area of interest requiring treatment. The screw includes an elongate shaft having a length extending between opposite ends. The shaft has an insulating coating extending along at least a portion of the length. The thickness of the insulating coating at various portions of the shaft is modulated to optimally direct current to a target area of interest requiring treatment. The controller adjusts the duty cycle of the current flow over the treatment period.

Certain embodiments of the invention relate to a surgical procedure resulting in the fusion of transverse processes. The disclosure herein presents novel approaches for accessing transverse processes of the spine, novel methods for the delivery of fusion material for the fusion of said transverse processes, and novel tools to facilitate the procedure. Certain embodiments of the invention include a graft delivery assembly, which has a delivery shaft, delivery sheath, and at least one curved rod. Bony material is position with a graft delivery assembly, in which retraction of the delivery shaft or sheath places the bone fusion material to the fusion site. The graft delivery assembly further includes features to decorticate and prepare the bone surface for fusion.

An implantable device including an intervertebral wedge including an upper bearing zone and a lower bearing zone and at least one first lateral spring having a position A relative to the intervertebral wedge in a position for inserting the implantable device and a position B relative to the intervertebral wedge in a position for implanting the implantable device, the positions A and B being different and the first lateral spring being configured: to freely translate from position A to position B and to form a retention component arranged relative to the intervertebral wedge to block the migration of the intervertebral wedge toward the spinal canal in position B.

The present invention provides a deformable body (2), wherein the deformable body comprises a force application surface (12) opposite a bone contact surface (52) to be pressed against periosteum of a bone surface (52) of a bone such that the bone contact surface adapts its shape to the shape of the bone surface, wherein the deformable body comprises one or more through-going openings (3) and/or one or more fixation locations (34) arranged to receive a fixation element such as as screw (20), and wherein the deformable body comprises an anaesthetic that is released from or through the bone contact surface. The anaesthetic can be bupivicaine, liposome bupivacaine, lidocaine or levobupivacaine. The anaestethic can be arranged in one or more compartments (6, 7) which have ifferent release rates. The screw can comprise a detent or rim to mate with the deformable body. A sleeve (80) can be arranged in the opening (3) to receive the screw. A pusher element (81) can push the deformable body from the sleeve into position on the screw.

The present invention relates to an interspinous integration type implant. Provided is an interspinous integration type implant which is an implant inserted between an upper spinous process and a lower spinous process and comprises: a spacer to which one end of an upper plate and one end of a lower plate are connected so as to be formed in a “” shape or “U” shape, and which is inserted between spinous processes in order to provide elasticity; an upper spinous process coupling means for tightly coupling the upper plate to the upper spinous process; and a lower spinous process coupling means for tightly coupling the lower plate to the lower spinous process, wherein the upper plate comprises at least one osseointegration hole formed to penetrate the top surface and the bottom surface of the upper plate so as to be moved by being integrated with the upper spinous process, and the lower plate comprises at least one osseointegration hole formed to penetrate the top surface and the bottom surface of the lower plate so as to be moved by being integrated with the lower spinous process. The interspinous integration type implant according to the present invention provides elasticity to the upper spinous process and the lower spinous process, thereby maintaining a space between the upper and lower spinous processes. Also, the interspinous integration type implant moves by being integrated with the upper and lower spinous processes through the osseointegration holes formed at the upper plate and the lower plate, and thus does not damage the spinous processes and has an effect of preventing a separation phenomenon from between the spinous processes. Also, the interspinous integration type implant has an effect of enabling minimally invasive surgery since blades can be rotated and tightened using an instrument after inserting the interspinous integration type implant from the side surface of spinous processes. Furthermore, after inserting the interspinous integration type implant between adjacent spinous processes and tightening the blades at both side surfaces of the spinous processes, a plurality of spikes provided in the blades are tightly embedded on the both side surfaces of the spinous processes, and thus there is an effect that an upper blade and a lower blade are stably coupled to the upper and lower spinous processes. In addition, since the interspinous integration type implant can be inserted between the spinous processes in a state where the upper blade an

The invention provides a hydrogel for in-vivo release of medication comprising at least one medication, wherein the surface of the hydrogel comprises a coating such that the surface has one or more sub-surfaces with permeability that is at least 2× higher than the average permeability of the entire surface, wherein the hydrogel has an elastic modulus of between 50 and 1000 kPa.