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FDA 510(k), K011584, MEDTRONIC SPINAL CORD STIMULATION AND PERIPHERAL NERVE STIMULATION SYSTEMS FOR PAIN RELIEF
FDA 510(k), K011584, MEDTRONIC SPINAL CORD STIMULATION AND PERIPHERAL NERVE STIMULATION SYSTEMS FOR PAIN RELIEF
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510(K) Number: K011584
Device Name: MEDTRONIC SPINAL CORD STIMULATION AND PERIPHERAL NERVE STIMULATION SYSTEMS FOR PAIN RELIEF
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: Stimulator, Spinal-Cord, Implanted (Pain Relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 05/23/2001
Decision Date: 06/22/2001
Regulation Medical Specialty: Neurology
Device Name: MEDTRONIC SPINAL CORD STIMULATION AND PERIPHERAL NERVE STIMULATION SYSTEMS FOR PAIN RELIEF
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: Stimulator, Spinal-Cord, Implanted (Pain Relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 05/23/2001
Decision Date: 06/22/2001
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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