PEZO INTERBODY CAGES SYSTEM

PEZO INTERBODY CAGES SYSTEM is an FDA 510(k)-cleared medical device (K103814) manufactured by Ulrich GmbH & Co. KG. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 16, 2011. Regulation: 8.