DePuy Synthes Trauma Screws

DePuy Synthes Trauma Screws is an FDA 510(k)-cleared medical device (K192745) manufactured by Synthes (Usa) Products, LLC / Depuy Orthopaedics, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 25, 2019. Regulation: 8.