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FDA 510(k), K030674, MODIFICATION TO AXXESS SPINAL CORD STIMULATION LEAD
FDA 510(k), K030674, MODIFICATION TO AXXESS SPINAL CORD STIMULATION LEAD
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$149.00 USD
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510(K) Number: K030674
Device Name: MODIFICATION TO AXXESS SPINAL CORD STIMULATION LEAD
Manufacturer: DREW JOHNSON
Device Classification Name: Stimulator, Spinal-Cord, Implanted (Pain Relief)
Regulation Number: GZB
Classification Product Code: 03/04/2003
Date Received: 03/28/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: MODIFICATION TO AXXESS SPINAL CORD STIMULATION LEAD
Manufacturer: DREW JOHNSON
Device Classification Name: Stimulator, Spinal-Cord, Implanted (Pain Relief)
Regulation Number: GZB
Classification Product Code: 03/04/2003
Date Received: 03/28/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
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