MICOMED POSTERIOR DOUBLEROD SYSTEM (MPDS)

MICOMED POSTERIOR DOUBLEROD SYSTEM (MPDS) is an FDA 510(k)-cleared medical device (K991862) manufactured by Micomed GmbH. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 12, 2000. Regulation: 8.