
Arthrex, Inc.
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MINI TIGHTROPE REPAIR KIT, MODEL AR-8911DS is an FDA 510(k)-cleared medical device (K061925) manufactured by Arthrex, 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 October 30, 2006. Regulation: 8.