G-FORCE GEN 2 SUTURE ANCHOR SYSTEM

G-FORCE GEN 2 SUTURE ANCHOR SYSTEM is an FDA 510(k)-cleared medical device (K141011) manufactured by Wrightmedicaltechnologyinc. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 29, 2014. Regulation: 8.