...fuse the sacroiliac (SI) joint and to serve as foundational support at the base of a spine fusion construct. The initial clearance included an indication for use with a single...
...treatment of sacroiliac joint dysfunction. The FDA 510(k) clearance is a very exciting step forward for patients who suffer from pain due to sacroiliac joint disruptions and degenerative sacroiliitis.” Source:...
...Sacroiliac Joint Fusion System is intended for sacroiliac joint fusion for conditions including degenerative sacroiliitis and sacroiliac joint disruption. The system consists of 3D Printed implants designed to transfix the...
...obstacles of the straight Lateral approach. The TransLoc 3D System is intended to fixate the sacroiliac (SI) joint with the long-term goal of fusion. These titanium 3D-printed devices are available...
Aurora Spine received FDA 510(k) clearance to market the minimally invasive SiLO TFX MIS Sacroiliac Joint Fixation System. SiLO TFX is intended for sacroiliac joint fusion for conditions including sacroiliac...
...drilling tool for sacroiliac joint fusion, both embedding the DSG (Dynamic Surgical Guidance) technology. It complements an existing network of agents and distributors commercializing PediGuard and DSG Connect, as well...
...Sacrix has developed percutaneous fluoroscopic lateral-oblique sacroiliac joint fusion technologies for the treatment of sacroiliac dysfunction and sacroiliitis, such as the SacroFuse threaded compression device. KICVentures sees this merger as...
...of the novel EVOL-SI Fusion System portfolio, which is designed to treat dysfunctions of the sacroiliac joint. The T-FIX 3DSI Joint Fusion System is FDA 510(k) cleared for multiple approaches:...
...competency has been within the interbody and sacroiliac (SI) fixation spaces. But we hold an intellectual property position relative to what I call futuristic fixation in the entire orthopedic arena,...
...2021, iFuse-TORQ has been used to treat many patients suffering from a pelvic fracture or sacroiliac joint dysfunction,” said Laura Francis, CEO of SI-BONE. “This pelvic fracture fixation indication expansion...
