MITEK SUPER QUICKANCHOR, MODIFICATION

MITEK SUPER QUICKANCHOR, MODIFICATION is an FDA 510(k)-cleared medical device (K930893) 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 December 7, 1993. Regulation: 8.