PRECISION Adverse Event — Injury (MDR 2029203-2008-00067)
PRECISION Adverse Event — Injury (MDR 2029203-2008-00067) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRECISION; Generic name: SPINAL CORD STIMULAR; Manufacturer: BOSTON SCIENTIFIC NEUROMODULATION CORP..
| Device | PRECISION |
|---|---|
| Generic name | SPINAL CORD STIMULAR |
| Manufacturer | BOSTON SCIENTIFIC NEUROMODULATION CORP. |
| Report number | 2029203-2008-00067 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-21 |
| Report source | Health Professional |
| Narrative | THE PT SYSTEM WAS EXPLANTED DUE TO INFECTION. THE PT WAS IMPLANTED WITH A NEW BOSTON SCIENTIFIC SPINAL CORD STIMULATOR SYSTEM. |
| Source | openFDA MAUDE (device adverse events) |
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