Medtronic Neurological
6 FDA 510(k) clearances · Recalling firm
◉ Watch Medtronic Neurological
| Record | Firm | Date |
|---|---|---|
| Medtronic Kinetra Dual Program Neurostimulator for Deep Brain Stimulation, model 7428. Rx recall (Z-0290-2007) | Medtronic Neurological | 2006-12-19 |
| Medtronic 3777 Lead Kit, 1x8 Low Impedance Lead Kit for Spinal Cord Stimulation (SCS). Man recall (Z-1536-06) | Medtronic Neurological | 2006-09-29 |
| Medtronic 3778 Lead Kit, 1x8 Compact Low Impedance Lead Kit for Spinal Cord Stimulation (S recall (Z-1537-06) | Medtronic Neurological | 2006-09-29 |
| Medtronic Intrathecal Catheter, Model 8731, (part of infusion systems using Medtronic impl recall (Z-1414-06) | Medtronic Neurological | 2006-09-09 |
| Medtronic Intrathecal Catheter Distal Revision Kit, Model 8598, (provides replacement part recall (Z-1415-06) | Medtronic Neurological | 2006-09-09 |
| Medtronic Kinetra 7428. Dual Program Neurostimulator for Deep Brain Stimulation. Rx only. recall (Z-0861-06) | Medtronic Neurological | 2006-05-27 |
Track Medtronic Neurological automatically
Every clearance here is in the API, with alerts when new ones post.