PMT SUBARACHNOID SCREW, MODEL NO.1350-2

PMT SUBARACHNOID SCREW, MODEL NO.1350-2 is an FDA 510(k)-cleared medical device (K883115) manufactured by Pmt 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 August 28, 1988. Regulation: 8.