EARP Interbody System

EARP Interbody System is an FDA 510(k)-cleared medical device (K212477) manufactured by Nvision Biomedical Technologies, Inc.. 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 27, 2022. Regulation: 8.