
Home » FDA Clears Orthofix’s Bone-Screw System for Sacroiliac Joint Dysfunction
FDA Clears Orthofix’s Bone-Screw System for Sacroiliac Joint Dysfunction
Orthofix has earned 510(k) clearance from the FDA for its Firebird sacroiliac joint-fusion system, an implant that compresses and stabilizes the joint.
The 3D-printed titanium device has a porous section that allows bone to grow into its surface, creating a bond between the implant and the bone at the sacroiliac joint.
The system is implanted during a minimally invasive surgery that takes about an hour.
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