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

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