Quattro Bolt Tenodesis Screw

Quattro Bolt Tenodesis Screw is an FDA 510(k)-cleared medical device (K143392) manufactured by Cayenne Medical, 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 January 22, 2015. Regulation: 8.