CERVICAL SELF-RETAINING RETRACTOR

CERVICAL SELF-RETAINING RETRACTOR is an FDA 510(k)-cleared medical device (K935529) manufactured by T. Korossurgical Instruments Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 21, 1994. Regulation: 8.