NuVasive Reline Cervical System

NuVasive Reline Cervical System is an FDA 510(k)-cleared medical device (K213654) 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 February 22, 2022. Regulation: 8.