Arthrex FiberTape Cerclage

Arthrex FiberTape Cerclage is an FDA 510(k)-cleared medical device (K170206) 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 November 14, 2017. Regulation: 8.