VERSATRAC (TM) LUMBAR RETRACTOR SYSTEM

VERSATRAC (TM) LUMBAR RETRACTOR SYSTEM is an FDA 510(k)-cleared medical device (K964402) manufactured by V. Mueller Neuro/Spine. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 22, 1997. Regulation: 8.