GRAVITY™ Syndesmosis LP

GRAVITY™ Syndesmosis LP is an FDA 510(k)-cleared medical device (K170249) 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 June 29, 2017. Regulation: 8.