SPECTRA WAVEWRITER Adverse Event — Injury (MDR 3006630150-2020-01901)
SPECTRA WAVEWRITER Adverse Event — Injury (MDR 3006630150-2020-01901) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SPECTRA WAVEWRITER; Generic name: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF; Manufacturer: BOSTON SCIENTIFIC NEUROMODULATION.
| Device | SPECTRA WAVEWRITER |
|---|---|
| Generic name | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
| Manufacturer | BOSTON SCIENTIFIC NEUROMODULATION |
| Report number | 3006630150-2020-01901 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | A REPORT WAS RECEIVED THAT THE PATIENT HAD AN INFECTION. THE PATIENT UNDERWENT A SPINAL CORD STIMULATOR (SCS) EXPLANT PROCEDURE. |
| Source | openFDA MAUDE (device adverse events) |
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