An instrument includes a sleeve extending between proximal and distal ends. The sleeve defines a passageway. The proximal end includes an aperture extending into an outer surface of the sleeve. The distal end includes an engagement surface and an opening extending through the engagement surface. The opening is in communication with the passageway. A member is movably disposed in the aperture. The member includes a spring and a body. The body defines a bore. A shaft extends between opposite proximal and distal ends. The proximal end of the shaft extends through the bore. The distal end of the shaft extends through the opening. Systems and methods of use are disclosed.

A disc implant device can be provided in a generally planar rectangular sheet having a first elongated side, a second elongated side opposing the first elongated side, a first end, and a second end opposing the first end. The generally planar rectangular sheet is structured with alternating segments of joint ridges, each segment of joint ridges being configured to form a spacing joint segment and alternating segments of arm ridges, each arm segment being configured to form a plurality of radially extending arms, the joint segments providing flexibility to the device. When the disc implant is folded or rolled from its planar configuration to a generally cylindrical configuration, the arm segments are axially collapsible and radially expandable such that in such a configuration, the implant includes segments of radially expanded arms separated by spacing joint segments.

A sacroiliac joint fusion screw and associated delivery tools and method. Embodiments of the sacroiliac joint fusion screw comprise a shaft having proximal and distal end portions and a head on the proximal end of the shaft. A threaded portion on a distal portion of the shaft is configured to engage a sacrum. A glide zone portion on the shaft between the threaded portion and the proximal end portion is configured to extend through an ilium. The screw can provide stability and compression to the joint.

Methods and devices for consistently and accurately controlling the depth of the graft tunnel. A sheath is inserted into the bone until a stop member on the sheath contacts the bone. A cutting member is then deployed to drill a larger bore in the tunnel until making contact with the distal end of the sheath. The cutting member may be drawn retrograde within the tunnel, or driven antegrade from an opening opposite the opening in which the sheath resides. The drill and the sheath can then be removed, leaving the tunnel that includes a tunnel portion sized to fit a graft so that the graft fits tightly within the tunnel portion and is flush with the opening of the tunnel.

An implant surgery drill capable of preventing accidents in advance by actively reinforcing coupling force between a cutting part for cutting the alveolar bone and a connecting part for connecting the cutting part to a handpiece is proposed. The drill can include a cutting part having a plurality of cutting blades that comprise saw teeth and are aligned in a circular shape so as to perforate the alveolar bone; and a connecting part interposed between the handpiece and the cutting part, wherein, specifically, the cutting part including: the saw teeth aligned in a circular shape at the upper end thereof; a cutting upper part extending downward from the saw teeth; and a cutting lower part protruding downward from the cutting upper part with an expanded diameter.

A drill device including a shaft having a proximal end and a distal end, one or more first reaming heads configured to be positioned along the shaft adjacent the distal end and one or more second reaming heads configured to be positioned along the shaft at a location axially proximally spaced from the first reaming head.

A tool configured to deliver a radially compressible hydrogel implant at a surgical site includes an introducer tube, a plunger provided inside the introducer tube and configured to travel from the proximal end of the introducer tube toward the distal end of the introducer tube urging the hydrogel implant through a sloped portion of the introducer tube radially compressing the implant before exiting through the distal end of the introducer tube, a handle connected to the introducer tube, and a clamp hingeably connected to the handle.

Illustrative embodiments of orthopedic implants and methods for surgically repairing hammertoe are disclosed. According to at least one illustrative embodiment, an orthopedic implant includes a proximal segment comprising a number of spring arms forming an anchored barb at a first end of the implant, a distal segment extending between the proximal segment and a second end of the implant, and a central segment disposed between the proximal and distal segment.

Methods and apparatuses for performing an orthopedic procedure in the sacroiliac region are disclosed. In one form, an aperture is formed that at least partially extends through at least one of an ilium and a sacrum. An undercutting system is inserted into the aperture. The undercutting system may include an insertion apparatus, a probe assembly, and a cutting assembly. The probe assembly is moved with respect to the insertion apparatus from a retracted position to an extended position. The probe assembly is manipulated within a joint between the ilium and the sacrum while the probe assembly is in the extended position. The cutting assembly is moved with respect to the insertion apparatus from a retracted position to an extended position. The cutting assembly is manipulated within the joint between the ilium and the sacrum while the cutting assembly is in the extended position to form a fusion region.

Methods of deploying an intravertebral implant having an expandable anterior part, a posterior part coupled to the expandable anterior part, and a pedicle fixation element. The expandable anterior part is positioned within the vertebral body, and the posterior part may be positioned within the vertebral body. The pedicle fixation element is anchored to the vertebral body. The expandable anterior part is moved relative to the pedicle fixation element, for example, in two degrees of freedom. Movement in a first of the two degrees of freedom is independent from movement in a second of the two degrees of freedom. The expandable anterior part may be translated without being rotated along a main axis of the pedicle fixation element. Filling material may be injected through the posterior part. Rotational movements of the expandable anterior part relative to the pedicle fixation element may be locked.