SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM

SYNTHES (USA) ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM is an FDA 510(k)-cleared medical device (K945700) 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 19, 1995. Regulation: 8.