Shoreline Cervical Interbody RT System

Shoreline Cervical Interbody RT System is an FDA 510(k)-cleared medical device (K183083) 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 February 13, 2019. Regulation: 8.