NuVasive BASE Interfixated Titanium System

NuVasive BASE Interfixated Titanium System is an FDA 510(k)-cleared medical device (K170592) 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 April 25, 2017. Regulation: 8.