Toro-L Interbody Fusion System

Toro-L Interbody Fusion System is an FDA 510(k)-cleared medical device (K213355) manufactured by Integrity Implants, 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 March 24, 2022. Regulation: 8.