FDA 510(k), K162741, AxoGuard Nerve Connector

FDA 510(k), K162741, AxoGuard Nerve Connector

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510(K) Number: K162741
Device Name: AxoGuard Nerve Connector
Manufacturer: COOK BIOTECH INCORPORATED
Device Classification Name: Cuff, Nerve
Regulation Number: 882.5275
Classification Product Code: JXI
Date Received: 09/30/2016
Decision Date: 10/31/2016
Regulation Medical Specialty: Neurology

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