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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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