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FDA 510(k), K934065, MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM
FDA 510(k), K934065, MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM
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510(K) Number: K934065
Device Name: MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 08/20/1993
Decision Date: 02/14/1995
Regulation Medical Specialty: Neurology
Device Name: MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM
Manufacturer: MEDTRONIC VASCULAR
Device Classification Name: stimulator, spinal-cord, implanted (pain relief)
Regulation Number: 882.5880
Classification Product Code: GZB
Date Received: 08/20/1993
Decision Date: 02/14/1995
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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