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FDA 510(k), K930242, INTRODE INT-8
FDA 510(k), K930242, INTRODE INT-8
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510(K) Number: K930242
Device Name: INTRODE INT-8
Manufacturer: NEUROMED, INC.
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 01/19/1993
Decision Date: 02/02/1994
Regulation Medical Specialty: Neurology
Device Name: INTRODE INT-8
Manufacturer: NEUROMED, INC.
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 01/19/1993
Decision Date: 02/02/1994
Regulation Medical Specialty: Neurology
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- 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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