AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV

AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV is an FDA 510(k)-cleared medical device (K030698) 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 March 19, 2003. Regulation: 8.