Anspach Helix Dissection Tools

Anspach Helix Dissection Tools is an FDA 510(k)-cleared medical device (K183545) 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 July 18, 2019. Regulation: 8.