SYNTHES ANTERIOR CERVICAL COMPRESSION SYSTEM

SYNTHES ANTERIOR CERVICAL COMPRESSION SYSTEM is an FDA 510(k)-cleared medical device (K033844) 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 February 4, 2004. Regulation: 8.