Codman Disposable Perforators

Codman Disposable Perforators is an FDA 510(k)-cleared medical device (K183581) manufactured by Integra Lifesciences 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 19, 2019. Regulation: 8.