NuVasive Modulus XLIF Interbody System

NuVasive Modulus XLIF Interbody System is an FDA 510(k)-cleared medical device (K201692) 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 28, 2020. Regulation: 8.