SPINAL USA ANTERIOR LUMBAR PLATE SYSTEM

SPINAL USA ANTERIOR LUMBAR PLATE SYSTEM is an FDA 510(k)-cleared medical device (K091044) manufactured by Spinal USA. 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 8, 2009. Regulation: 8.