FuzeFix Screw System – FDA Cleared

We are pleased to announce the FuzeFix Screw system as the newest addition to the FDA cleared Fusion Orthopedics product offering.  FDA 510(k) approval was issued August 7, 2017. The assigned FDA 510(k) # for the FuzeFix Screw System is K170038. The FuzeFix Screw System consists of: Headed Compression Screws from...