In some aspects, a device comprising an implant configured for insertion into a portion of human anatomy, and at least one covering coupled to the implant is provided. According to some aspects, the implant comprises one or more protrusions configured to prevent leakage of material and/or to resist displacement of the implant. According to some aspects, the covering is configured to facilitate improved leakage and/or implant displacement prevention.

Provided herein are devices, systems, apparatus and methods for accessing the cervical spine via an anterior approach and implanting a spinal fixation member between two vertebrae of the cervical spine in the disc or intervertebral joint space, such as in an ACDF procedure. The delivery device includes a distal end that can be anchored to the spinal fixation member. Once anchored to the spinal fixation member, the delivery device is operable to both advance and attach the spinal fixation member within a cervical disc joint space.

The present invention provides an expandable fusion device capable of being installed inside an intervertebral disc space to maintain normal disc spacing and restore spinal stability, thereby facilitating an intervertebral fusion. In an exemplary embodiment, the present invention provides an intervertebral implant. The intervertebral implant may be configured to transition from a collapsed configuration having a first height and a first width to an expanded configuration having a second height and a second width.

An intervertebral implant for implantation in an intervertebral space between vertebrae. The implant includes a body extending from an upper surface to a lower surface. The body has a front end, a rear end and a pair of spaced apart first and second side walls extending between the front and rear walls such that an interior chamber is defined within the front and rear ends and the first and second walls. The body defines an outer perimeter and an inner perimeter extending about the internal chamber. At least one of the side walls is defined by a solid support structure and an integral porous structure, the porous structure extending from the outer perimeter to the inner perimeter. The porous structure embeds or encapsulates at least a portion of the solid support structure.

An orthopaedic implant includes: a first porous ingrowth material region; a second porous ingrowth material region coupled to the first porous ingrowth material region; and an intermediate region disposed between the first porous ingrowth material region and the second porous ingrowth material region. The intermediate region has a stiffness that differs from at least one of the first porous ingrowth material region or the second porous ingrowth material region.

Embodiments are directed to spinal treatments and, more particularly, to a trial inserter tool compatible with detachable trial heads for use in spinal surgery. In a preferred embodiment, the present invention provides a system for sizing an implant to be used in posterior lumbar interbody fusion surgery. The system may comprise a trial inserter tool, wherein the trial inserter tool comprises: a body, wherein the body is an elongated tubular, wherein the body comprises a first end and a second end; an actuation device, wherein the actuation device is disposed on the body between the first end and the second end; and a hooked support member that extends from the second end of the body; and a trial head disposable on the hooked support member.

A spinal implant includes a first member having a wall that defines an axial cavity. A second member extends between a first end and a second end and defines a longitudinal axis. The second member is configured for disposal with the axial cavity and translation relative to the first member. A third member has an outer surface engageable with tissue and an inner surface disposed to dynamically engage the first end in response to the engagement of the outer surface with the tissue. Systems and methods are disclosed.

A spinal implant device identifiable after implantation comprises an outer cage member and an implant body. The implant body is disposed between a first vertebra end and a second vertebra end of the outer cage and defines a plurality of planes. Each of the planes comprises separately readable indicia such that the indicia are discernible by at least one of x-ray, fluoroscopy, computed tomography, electromagnetic radiation, ultrasound, or magnetic resonance imaging.

A lumbar spine implant has a body with bone screw bores that angle from a metal faceplate situated at an end of the body, the bone screw bores sized such that the bone screw bores become threaded during introduction of a bone screw thereby providing a locking mechanism to prevent the bone screw from backing out. The faceplate also provides a pocket for each bone screw that prevents the bone screw head from advancing through the implant body. The lumbar spine implant has four bone screw bores, two of which extend from the faceplate to the upper side of the body, and two of which extend from the faceplate to the lower side of the body. More or less bone screw bores may be provided. Preferably, but not necessarily, the direction of the bone screw bores are staggered from one lateral side to another lateral side of the body.

Methods of reducing loading across a cartilaginous joint, or of reducing pain in a cartilaginous joint caused by cartilage damage in the joint. The methods involve implanting one or more magnetic devices in the bones, or affixing one or more magnetic devices onto the surface of the bones, that form the joint. For example, to reduce loading or reduce pain in a knee joint, one or more magnetic devices maybe implanted in the femur and in the tibia. The magnetic devices are oriented to generate a repulsive magnetic force between the one or more magnetic devices of each of the bones forming the joint.