Z-PLATE ANTERIOR FIXATION SYSTEM

Z-PLATE ANTERIOR FIXATION SYSTEM is an FDA 510(k)-cleared medical device (K922543) manufactured by Sofamor Danek Mfg., Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 18, 1993. Regulation: 8.