XIHPOS™ ZFUZE™ Interbody Fusion System

XIHPOS™ ZFUZE™ Interbody Fusion System is an FDA 510(k)-cleared medical device (K190544) manufactured by Difusion Technologies. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 31, 2019. Regulation: 8.