
Aesculap, Inc.
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AESCULAP ORTHOPILOT 2 THA V 2.0 is an FDA 510(k)-cleared medical device (K050752) 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 April 26, 2005. Regulation: 8.