
Micro Therapeutics, Inc.
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SAPPHIRE DETACHABLE FIBERED COIL SYSTEM, HELIX FIBERED, CYCLONE, MULTIPLE MODELS is an FDA 510(k)-cleared medical device (K033372) manufactured by Micro Therapeutics, 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 January 8, 2004. Regulation: 8.