MITEK ANCHOR(TM)

MITEK ANCHOR(TM) is an FDA 510(k)-cleared medical device (K897155) 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 April 3, 1990. Regulation: 8.