FDA 510(k), K011168, NEUROGEN NERVE GUIDE

FDA 510(k), K011168, NEUROGEN NERVE GUIDE

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510(K) Number: K011168
Device Name: NEUROGEN NERVE GUIDE
Manufacturer: INTEGRA LIFESCIENCES CORP.
Device Classification Name: Cuff, Nerve
Regulation Number: 882.5275
Classification Product Code: JXI
Date Received: 04/17/2001
Decision Date: 06/22/2001
Regulation Medical Specialty: Neurology

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