ANSPACH ACCESS CRANIAL PERFORATOR

ANSPACH ACCESS CRANIAL PERFORATOR is an FDA 510(k)-cleared medical device (K982991) 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 October 20, 1998. Regulation: 8.