MITEK MINI QUICKANCHOR PLUS

MITEK MINI QUICKANCHOR PLUS is an FDA 510(k)-cleared medical device (K992487) manufactured by Mitek Products. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 20, 1999. Regulation: 8.