SYNTHES HINDFOOT ARTHRODESIS NAIL SYSTEM

SYNTHES HINDFOOT ARTHRODESIS NAIL SYSTEM is an FDA 510(k)-cleared medical device (K051678) 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 20, 2005. Regulation: 8.