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Advanced Neuromodulation System,Inc
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LAMITRODE S-SERIES (S4 AND S8) LEADS is an FDA 510(k)-cleared medical device (K022222) manufactured by Advanced Neuromodulation System,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 August 7, 2002. Regulation: 8.