STREAMLINE OCT OCCIPITO-CERVICO-THORACIC SYSTEM

STREAMLINE OCT OCCIPITO-CERVICO-THORACIC SYSTEM is an FDA 510(k)-cleared medical device (K133374) manufactured by Pioneer Surgical Technology, Inc. (Rti Surgical, I. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 2014. Regulation: 8.