ANSPACH MRI SAFE SURGICAL DRILL SYSTEM

ANSPACH MRI SAFE SURGICAL DRILL SYSTEM is an FDA 510(k)-cleared medical device (K040186) manufactured by The Anspach Effort, 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 April 14, 2004. Regulation: 8.