
T.A.G. Medical Products Corporation, Ltd.
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KNOTILUS ANCHOR SYSTEM is an FDA 510(k)-cleared medical device (K113297) manufactured by T.A.G. Medical Products Corporation, Ltd.. 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 1, 2012. Regulation: 8.