STRYKER WEDGE SUTURE ANCHOR

STRYKER WEDGE SUTURE ANCHOR is an FDA 510(k)-cleared medical device (K983557) manufactured by Stryker Endoscopy. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 17, 1998. Regulation: 8.