NuVasive VuePoint II OCT System

NuVasive VuePoint II OCT System is an FDA 510(k)-cleared medical device (K150474) 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 20, 2015. Regulation: 8.