Medtronic Inc, Neurological & Spinal Division
6 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Medtronic Model 37711 Restore Neurostimulator. The Restore Neurostimulator is an implanted recall (Z-0905-06) | Medtronic Inc, Neurological & Spinal Division | 2006-05-25 |
| Medtronic Activa Deep Brain Stimulation (DBS) system including the following system compon recall (Z-0370-06) | Medtronic Inc, Neurological & Spinal Division | 2006-01-10 |
| Model 8561 Lioresal (Baclofen injection) Intrathecal Refill Kit is designed for refilling recall (Z-0391-05) | Medtronic Inc, Neurological & Spinal Division | 2005-01-13 |
| 8870 software application card versions AAA 02, BBB 04, BBC 02, and BBD 01, which is used recall (Z-1334-04) | Medtronic Inc, Neurological & Spinal Division | 2004-09-23 |
| The Model 8540 Catheter Access Port Kit is intended for use in accessing the catheter via recall (Z-1384-04) | Medtronic Inc, Neurological & Spinal Division | 2004-08-24 |
| Synchromed II infusion pump recall (Z-1040-04) | Medtronic Inc, Neurological & Spinal Division | 2004-07-20 |
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Every clearance here is in the API, with alerts when new ones post.