DEPUY SYNTHES MAXFRAME AUTOSTRUT System

DEPUY SYNTHES MAXFRAME AUTOSTRUT System is an FDA 510(k)-cleared medical device (K231922) manufactured by DePuy Synthes. 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 25, 2023. Regulation: 8.