Meridian Anterior Plate System, Regatta Lateral Plate System

Meridian Anterior Plate System, Regatta Lateral Plate System is an FDA 510(k)-cleared medical device (K200885) manufactured by SeaSpine Orthopedics Corporation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 27, 2020. Regulation: 8.