NEDBOND EJECTOR KERRISON RONGEUR

NEDBOND EJECTOR KERRISON RONGEUR is an FDA 510(k)-cleared medical device (K933978) manufactured by Redmond Neurotechnologies 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 January 11, 1994. Regulation: 8.