MODULOCK POSTERIOR SPINAL FIXATION

MODULOCK POSTERIOR SPINAL FIXATION is an FDA 510(k)-cleared medical device (K902397) 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 November 4, 1990. Regulation: 8.