MODIFICATION TO GHAJAR GUIDE TWIST DRILL

MODIFICATION TO GHAJAR GUIDE TWIST DRILL is an FDA 510(k)-cleared medical device (K932402) manufactured by Neurodynamics, 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 August 4, 1993. Regulation: 8.