MODOFOCATION TO SYNTHES ANKLE ARTHRODESIS PLATES

MODOFOCATION TO SYNTHES ANKLE ARTHRODESIS PLATES is an FDA 510(k)-cleared medical device (K022255) 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 July 24, 2002. Regulation: 8.