Smith & Nephew Intramedullary Nail Systems

Smith & Nephew Intramedullary Nail Systems is an FDA 510(k)-cleared medical device (K210980) manufactured by Smith & Nephew, 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 13, 2022. Regulation: 8.