NuVasive CoRoent Small Interlock System

NuVasive CoRoent Small Interlock System is an FDA 510(k)-cleared medical device (K192582) 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 November 12, 2019. Regulation: 8.