CurvaFix Receives FDA 510(k) Clearance for CurvaFix Rodscrew Company’s Innovative Curved Device to aid Orthopedic Trauma Surgery


BELLEVUE, Wash., March 05, 2019 (GLOBE NEWSWIRE) — CurvaFix, Inc., a developer of medical devices to repair bone fractures in orthopedic trauma patients, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the CurvaFix® Intramedullary Rodscrew. CurvaFix’s patented solution has the potential to improve outcomes and enable a less invasive approach in…

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