
Mri Interventions, Inc.
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MRII CRAINIAL DRILL is an FDA 510(k)-cleared medical device (K122456) manufactured by Mri Interventions, 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 March 21, 2013. Regulation: 8.