INTERSTIM Adverse Event — Injury (MDR 2182207-2008-00779)
INTERSTIM Adverse Event — Injury (MDR 2182207-2008-00779) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INTERSTIM; Manufacturer: MEDTRONIC NEUROMODULATION; Report number: 2182207-2008-00779.
| Device | INTERSTIM |
|---|---|
| Manufacturer | MEDTRONIC NEUROMODULATION |
| Report number | 2182207-2008-00779 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Study, Literature, Health Professional |
| Narrative | JOURNAL REF: ABOSEIF ET AL. "SACRAL NEUROMODULATION: COST CONSIDERATION AND CLINICAL BENEFIT." JOURNAL OF UROLOGY. 2007; 70:1069-1074. THE PURPOSE OF THE STUDY WAS TO DEMONSTRATE THE EFFICACY OF SACRAL NEUROMODULATION AND COMPARE VOIDING-RELATED HEALTH CARE UTILIZATION COSTS BEFORE AND AFTER RECEIVING AN INTERSTIM IMPLANT. A RETROSPECTIVE REVIEW OF 65 PTS RECEIVING INTERSTIM THERAPY WAS COMPLETED. |
| Source | openFDA MAUDE (device adverse events) |
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