Interbody Fusion (IBF)/Vertebral Body Replacement (VBR) System

Interbody Fusion (IBF)/Vertebral Body Replacement (VBR) System is an FDA 510(k)-cleared medical device (K170643) manufactured by Rti Surgical, Inc. Dba Rti Biologics. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 13, 2017. Regulation: 8.