TEW CRANIAL/SPINAL RETRACTOR MODEL A1090

TEW CRANIAL/SPINAL RETRACTOR MODEL A1090 is an FDA 510(k)-cleared medical device (K960807) manufactured by Ohio Medical Instrument Co., Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 16, 1996. Regulation: 8.