Aesculap, Inc.
AESCULAP -MIETHKE SHUNT SYSTEM
SKU K011030UPC JXG
In Stock
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IIFDA 510(k) Cleared (K011030)
1
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Aesculap, Inc.
Free shipping on orders over $99 · 30-day returns
AESCULAP -MIETHKE SHUNT SYSTEM is an FDA 510(k)-cleared medical device (K011030) 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 February 28, 2002. Regulation: 8.
