Streamline OCT Occipito-Cervico-Thoracic System

Streamline OCT Occipito-Cervico-Thoracic System is an FDA 510(k)-cleared medical device (K150254) manufactured by Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.). This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 27, 2015. Regulation: 8.