Abstract: A sacroiliac joint implant system includes a primary implant configured to be received in a sacroiliac joint of a patient and a secondary implant configured to couple with the primary implant. The primary implant includes a body extending from a proximal end to a distal end and a plurality of threads extending from the body. The secondary implant includes a first anchor configured to anchor within a sacrum of the patient and a second anchor configured to anchor within an ilium of the patient.

Abstract: A sacroiliac joint implant system includes a primary implant configured to be received in a sacroiliac joint of a patient and a secondary implant configured to couple with the primary implant. The primary implant includes a body extending from a proximal end to a distal end and a plurality of threads extending from the body. The secondary implant includes a first anchor configured to anchor within a sacrum of the patient and a second anchor configured to anchor within an ilium of the patient.

Abstract: A sacroiliac joint implant system includes a primary implant configured to be received in a sacroiliac joint of a patient and a secondary implant configured to couple with the primary implant. The primary implant includes a body extending from a proximal end to a distal end and a plurality of threads extending from the body. The secondary implant includes a first anchor configured to anchor within a sacrum of the patient and a second anchor configured to anchor within an ilium of the patient.

Abstract: A sacroiliac joint implant system includes a primary implant configured to be received in a sacroiliac joint of a patient and a secondary implant configured to couple with the primary implant. The primary implant includes a body extending from a proximal end to a distal end and a plurality of threads extending from the body. The secondary implant includes a first anchor configured to anchor within a sacrum of the patient and a second anchor configured to anchor within an ilium of the patient.

Abstract: A particle comprising hydroxyapatite, ?-tricalcium phosphate, ?-tricalcium phosphate, and/or bioactive glass is provided. The particle can be useful in bone graft compositions further comprising a carrier. The composition can include a quadphasic particle having hydroxyapatite, ?-tricalcium phosphate, ?-tricalcium phosphate, bioactive glass, and a carrier. The particle can have a size in the range of 50 microns to 2.5 mm. A method of repairing a bone defect is also provided. The method can include a step of applying the bone graft composition to a subject having the bone defect, such as a spinal bone defect. The subject receiving the bone graft composition can be a mammal, namely a human, pet, or domestic animal.

Abstract: A method for implanting an intrafacet implant includes making an incision, advancing an instrument assembly through the incision and to a facet joint. The instrument assembly includes a guide having a lumen extending therethrough. The method includes anchoring the guide at the facet joint, advancing an intrafacet implant to the facet joint through the guide using an inserter, and countersinking the intrafacet implant within the facet joint using the inserter.

Abstract: A bone graft delivery system includes a rasp having an elongate body extending between a proximal end and a distal end, a lumen extending through the elongate body and configured to receive bone graft material, a rasping surface removably couplable to the distal end of the elongate body and configured to decorticate bone material of a patient, and one or more openings configured to deliver bone graft material from the lumen.

Abstract: A bone graft delivery system can include an elongate tube and a handle having a trigger and a ratcheting mechanism. The trigger is actuated to deliver bone graft material through the tube. The bone graft delivery system can further include a distal tip at a distal end of the tube. The tip has one or more openings to deliver the bone graft material to a desired location and includes a surface suitable to act as a rasp for decorticating bone. A method for delivering bone graft material to a desired surgical location includes providing a bone graft delivery device, positioning the device adjacent the surgical location, decorticating bone, and delivering bone graft material to the surgical location.

Abstract: A bone graft delivery system can include an elongate tube and a handle having a trigger and a ratcheting mechanism. The trigger is actuated to deliver bone graft material through the tube. The bone graft delivery system can further include a distal tip at a distal end of the tube. The tip has one or more openings to deliver the bone graft material to a desired location and includes a surface suitable to act as a rasp for decorticating bone. A method for delivering bone graft material to a desired surgical location includes providing a bone graft delivery device, positioning the device adjacent the surgical location, decorticating bone, and delivering bone graft material to the surgical location.

Abstract: A bone graft delivery system includes a rasp having an elongate body extending between a proximal end and a distal end, a lumen extending through the elongate body and configured to receive bone graft material, a rasping surface removably couplable to the distal end of the elongate body and configured to decorticate bone material of a patient, and one or more openings configured to deliver bone graft material from the lumen.

Abstract: The devices and methods described herein refer to a guidewire, sometimes referred to as a K-wire, for use during varying orthopedic surgeries. The guidewire allows for the measurement of objects and distances inside the patient's body when used in tandem with x-ray or fluoroscopy imaging. Also, the devices and methods described herein act as a guide to accurately insert an instrument or implant, in the correct orientation, to the surgical site. The guidewire comprises a measurement segment that comprises one or more markers placed at known distances from the distal end of the guidewire. The markers, when used in tandem with fluoroscopy and/or x-ray imaging, provide users with a reference for measuring objects and distances inside the body. The markers can have many possible designs or configurations such as, but not limited to, visualization windows, grooves, notches, and/or material inserts.

Abstract: A bone graft delivery system includes a rasp having an elongate body extending between a proximal end and a distal end, a lumen extending through the elongate body and configured to receive bone graft material, a rasping surface removably couplable to the distal end of the elongate body and configured to decorticate bone material of a patient, and one or more openings configured to deliver bone graft material from the lumen.

Abstract: A bone graft delivery system includes an elongate tube configured to couple to the handle and receive a bone graft material and a rasp. The rasp includes a lumen configured to receive at least a portion of the elongate tube, a rasping surface configured to decorticate bone, one or more openings configured to deliver bone graft material from the elongate tube when the lumen receives at least a portion of the elongate tube, and a handle portion configured to be gripped in use to facilitate movement of the rasping surface to decorticate bone.

Abstract: A method for delivering bone graft material includes removing a container housing a bone graft material from a cryopreservation environment, wherein the bone graft material includes cellular matrix. The container includes an elongate tubular body having a first opening on a first end and a second opening on the second end. The container includes a first cap covering the first opening and a second cap covering the second opening. The method includes placing the container within a bath, removing the container from the bath, removing the first cap and the second cap from the elongate tubular body, coupling the elongate tubular body to a body of a bone graft delivery device while the bone graft material is positioned within the elongate tubular body, and delivering bone graft material through the elongate tubular body to a surgical location using the bone graft delivery device.

Abstract: A bone graft delivery system includes an elongate tube configured to couple to the handle and receive a bone graft material and a rasp. The rasp includes a lumen configured to receive at least a portion of the elongate tube, a rasping surface configured to decorticate bone, one or more openings configured to deliver bone graft material from the elongate tube when the lumen receives at least a portion of the elongate tube, and a handle portion configured to be gripped in use to facilitate movement of the rasping surface to decorticate bone.

Abstract: A bone graft delivery system can include an elongate tube and a handle having a trigger and a ratcheting mechanism. The trigger is actuated to deliver bone graft material through the tube. The bone graft delivery system can further include a distal tip at a distal end of the tube. The tip has one or more openings to deliver the bone graft material to a desired location and includes a surface suitable to act as a rasp for decorticating bone. A method for delivering bone graft material to a desired surgical location includes providing a bone graft delivery device, positioning the device adjacent the surgical location, decorticating bone, and delivering bone graft material to the surgical location.

Abstract: A bone graft delivery system can include an elongate tube and a handle having a trigger and a ratcheting mechanism. The trigger is actuated to deliver bone graft material through the tube. The bone graft delivery system can further include a distal tip at a distal end of the tube. The tip has one or more openings to deliver the bone graft material to a desired location and includes a surface suitable to act as a rasp for decorticating bone. A method for delivering bone graft material to a desired surgical location includes providing a bone graft delivery device, positioning the device adjacent the surgical location, decorticating bone, and delivering bone graft material to the surgical location.

Abstract: The devices and methods described herein refer to a guidewire, sometimes referred to as a K-wire, for use during varying orthopedic surgeries. The guidewire allows for the measurement of objects and distances inside the patient's body when used in tandem with x-ray or fluoroscopy imaging. Also, the devices and methods described herein act as a guide to accurately insert an instrument or implant, in the correct orientation, to the surgical site. The guidewire comprises a measurement segment that comprises one or more markers placed at known distances from the distal end of the guidewire. The markers, when used in tandem with fluoroscopy and/or x-ray imaging, provide users with a reference for measuring objects and distances inside the body. The markers can have many possible designs or configurations such as, but not limited to, visualization windows, grooves, notches, and/or material inserts.

Abstract: The headache mitigating apparatus includes at least a transverse strap configured to wrap around a user's head in the manner of a hat band and at least one strap configured to extend under the user's occipital bone and rest along the user's upper neck as well as extending over the head strap at a forward end thereof. The apparatus can include bladders in the transverse and occipital straps, respectively. The bladders can be filled simultaneously or separately with a pneumatic hand pump such as those found on sphygmomanometers or may include an inflation apparatus which is operable via a push button, in a manner similar to that in which self-inflating items inflate. At least one strap may also accommodate a gel pack for heating or cooling. One or both straps may include buckles or hook and loop closures configured to be adjusted to secure the apparatus to the user's head.