NuVasive Modulus-C Interbody System

NuVasive Modulus-C Interbody System is an FDA 510(k)-cleared medical device (K223731) manufactured by Nuvasive, 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 January 11, 2023. Regulation: 8.