MITEK MINI ANCHOR, MODIFICATION

MITEK MINI ANCHOR, MODIFICATION is an FDA 510(k)-cleared medical device (K930892) 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 January 6, 1994. Regulation: 8.