SYNTHES ANKLE ARTHRODESIS PLATE

SYNTHES ANKLE ARTHRODESIS PLATE is an FDA 510(k)-cleared medical device (K013415) 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 January 10, 2002. Regulation: 8.