MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM

MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM is an FDA 510(k)-cleared medical device (K012305) manufactured by Sulzer Spine-Tech. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 21, 2001. Regulation: 8.