MEDTRONIC NAVIGATION Adverse Event — Malfunction (MDR 1723170-2020-01312)
MEDTRONIC NAVIGATION Adverse Event — Malfunction (MDR 1723170-2020-01312) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MEDTRONIC NAVIGATION; Generic name: ORTHOPEDIC STEREOTAXIC INSTRUMENT; Manufacturer: MEDTRONIC NAVIGATION, INC.
| Device | MEDTRONIC NAVIGATION |
|---|---|
| Generic name | ORTHOPEDIC STEREOTAXIC INSTRUMENT |
| Manufacturer | MEDTRONIC NAVIGATION, INC |
| Report number | 1723170-2020-01312 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | DISTRIBUTOR, FOREIGN |
| Narrative | AT THE TIME OF FILING THIS INFORMATION WAS NOT AVAILABLE. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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