BRYAN POSTERIOR SPINAL FIXATOR (BPSF), MODIFIED

BRYAN POSTERIOR SPINAL FIXATOR (BPSF), MODIFIED is an FDA 510(k)-cleared medical device (K971457) manufactured by Arcan Orthopaedic Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 15, 1997. Regulation: 8.