AESCULAP-MEITHKE PROSA ADJUSTABLE SHUNT SYSTEM

AESCULAP-MEITHKE PROSA ADJUSTABLE SHUNT SYSTEM is an FDA 510(k)-cleared medical device (K120559) 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 May 23, 2012. Regulation: 8.