NuVasive CoRoent Small Interlock II System

NuVasive CoRoent Small Interlock II System is an FDA 510(k)-cleared medical device (K170961) 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 June 7, 2017. Regulation: 8.