MITEK TOGGLE ANCHOR(TM)

MITEK TOGGLE ANCHOR(TM) is an FDA 510(k)-cleared medical device (K950070) 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 May 21, 1995. Regulation: 8.