INTERFORM INTERBODY CAGE SYSTEM

INTERFORM INTERBODY CAGE SYSTEM is an FDA 510(k)-cleared medical device (K131082) manufactured by Next Orthosurgical. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 25, 2013. Regulation: 8.