ORTHOLOC ADVANTIM PS LSI TIBIAL INSERT

ORTHOLOC ADVANTIM PS LSI TIBIAL INSERT is an FDA 510(k)-cleared medical device (K940235) 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 October 4, 1994. Regulation: 8.