TRUMATCH Personalized Solutions

TRUMATCH Personalized Solutions is an FDA 510(k)-cleared medical device (K193540) manufactured by DePuy Orthopaedics, 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 June 15, 2020. Regulation: 8.