SYNTHES LCP ANKLE ARTHRODESIS PLATES

SYNTHES LCP ANKLE ARTHRODESIS PLATES is an FDA 510(k)-cleared medical device (K061940) manufactured by Synthes (Usa). This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 7, 2006. Regulation: 8.