MITEK G III ANCHOR, MITEK LS ANCHOR

MITEK G III ANCHOR, MITEK LS ANCHOR is an FDA 510(k)-cleared medical device (K944936) 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 March 23, 1995. Regulation: 8.