MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 1998-03-05 for MEDTRONIC 3982 manufactured by .
| Report Number | 2182207-1998-00046 |
| MDR Report Key | 154615 |
| Report Source | 05 |
| Date Received | 1998-03-05 |
| Date of Event | 1998-02-09 |
| Date Mfgr Received | 1998-02-13 |
| Date Added to Maude | 1998-03-10 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MEDTRONIC |
| Product Code | LHG |
| Date Received | 1998-03-05 |
| Model Number | 3982 |
| Device Eval'ed by Mfgr | R |
| Implant Flag | Y |
| Device Sequence No | 1 |
| Device Event Key | 150618 |
| Baseline Brand Name | SYMMIX |
| Baseline Generic Name | SURGICAL EPIDURAL LEAD |
| Baseline Model No | 3982 |
| Baseline Catalog No | NA |
| Baseline ID | NA |
| Baseline Device Family | STIM SYMMIX LEAD |
| Baseline Shelf Life Contained | Y |
| Baseline Shelf Life [Months] | 48 |
| Baseline PMA Flag | N |
| Baseline 510K PMN | Y |
| Premarket Notification | K913934 |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1998-03-05 |