LUQUE SEGMENTAL SPINAL INSTRUMENTATION

LUQUE SEGMENTAL SPINAL INSTRUMENTATION is an FDA 510(k)-cleared medical device (K913561) manufactured by Zimmer, 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 January 15, 1992. Regulation: 8.