FDA 510(k), K853643, MULTISTIM LAMINECTOMY ELECTRODE
FDA 510(k), K853643, MULTISTIM LAMINECTOMY ELECTRODE
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510(K) Number: K853643
Device Name: MULTISTIM LAMINECTOMY ELECTRODE
Manufacturer: NEUROMED, INC.
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 09/03/1985
Decision Date: 11/14/1985
Regulation Medical Specialty: Neurology
Device Name: MULTISTIM LAMINECTOMY ELECTRODE
Manufacturer: NEUROMED, INC.
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 09/03/1985
Decision Date: 11/14/1985
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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