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...
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HammerTech Fixation System – FDA Cleared
We are pleased to announce the HammerTech Fixation System as a new addition to the Fusion Orthopedics product offering. FDA 510(k) clearance was issued October 11th, 2016. The assigned FDA 510(k) # for the HammerTech Fixation System is K161449. The HammerTech device is indicated for the fixation of osteotomies and reconstruction...