NuVasive® Modulus TLIF Interbody System

NuVasive® Modulus TLIF Interbody System is an FDA 510(k)-cleared medical device (K172341) manufactured by Nu Vasive, Incorporated. 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 25, 2017. Regulation: 8.