G3¿ Active Plate® Large Fragment System

G3¿ Active Plate® Large Fragment System is an FDA 510(k)-cleared medical device (K152242) manufactured by Genesis Fracture Care, 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 23, 2015. Regulation: 8.