TORNIER INSITE(TM) FT PEEK KNOTLESS SUTURE ANCHOR

TORNIER INSITE(TM) FT PEEK KNOTLESS SUTURE ANCHOR is an FDA 510(k)-cleared medical device (K133777) manufactured by Tornier, 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 April 3, 2014. Regulation: 8.