Case Report
New Onset Tinnitus after High-Frequency Spinal Cord Stimulator Implantation
Table 2
Total number of adverse events reported to FDA MAUDE database by device.
| Nevro Senza HF10 | 903 | St. Jude Eon Mini | 1213 | St. Jude Protégé | 174 | St. Jude Proclaim | 63 | St Jude Prodigy | 32 | Medtronic Restore | 17 | Medtronic Restore Sensor | 1 | Boston Scientific Spectra | 2 | Boston Scientific Precision | 3 |
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