Medtronic, Inc. - Neuromodulation
6 FDA 510(k) clearances · Recalling firm
◉ Watch Medtronic, Inc. - Neuromodulation
| Record | Firm | Date |
|---|---|---|
| Medtronic SynchroMed II, Model 8637, (The SynchroMed II Pump is supplied in 20 ml or 40 ml recall (Z-3043-2011) | Medtronic, Inc. - Neuromodulation | 2011-08-29 |
| Medtronic SynchroMed II (Model No: 8637) implantable drug pump The SynchroMed II Programma recall (Z-1060-2011) | Medtronic, Inc. - Neuromodulation | 2011-02-10 |
| Medtronic SynchroMed implantable drug pump Refill Kits (Model No: 8551, 8555, 8561, 8562, recall (Z-1061-2011) | Medtronic, Inc. - Neuromodulation | 2011-02-10 |
| Medtronic SynchroMed EL (Model No: 8626 and 8627) implantable drug pump The SynchroMed EL recall (Z-1062-2011) | Medtronic, Inc. - Neuromodulation | 2011-02-10 |
| Medtronic Intrathecal Catheter, 8731SC with sutureless connector. Method of Sterilization: recall (Z-0334-2011) | Medtronic, Inc. - Neuromodulation | 2010-11-09 |
| Medtronic Intrathecal Catheter Spinal Segment Revision Kit, 8598A. Method of Sterilization recall (Z-0335-2011) | Medtronic, Inc. - Neuromodulation | 2010-11-09 |
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Every clearance here is in the API, with alerts when new ones post.