Miethke Shunt System GAV 2.0 and SA 2.0 Valves

Miethke Shunt System GAV 2.0 and SA 2.0 Valves is an FDA 510(k)-cleared medical device (K190174) manufactured by Aesculap, 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 4, 2019. Regulation: 8.