SYNTHES SPINE POSTERIOR CERVICAL/THORACIC HOOK/ROD SYSTEM

SYNTHES SPINE POSTERIOR CERVICAL/THORACIC HOOK/ROD SYSTEM is an FDA 510(k)-cleared medical device (K980358) 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 April 15, 1998. Regulation: 8.