DANEK SACRAL HOOK, MODIFICATION

DANEK SACRAL HOOK, MODIFICATION is an FDA 510(k)-cleared medical device (K911379) manufactured by Danek Medical, 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 September 10, 1991. Regulation: 8.