MITEK BONE ANCHOR, MODIFICATION

MITEK BONE ANCHOR, MODIFICATION is an FDA 510(k)-cleared medical device (K915889) manufactured by Mitek Surgical Products, 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 October 21, 1992. Regulation: 8.