510(k) K190504 ยท GXI Probe, Radiofrequency Lesion
Intracept Intraosseous Nerve Ablation System (RF Probe), Intracept Intraosseous Nerve Ablation System (Access Instruments), Relievant RF Generator
| Applicant | Relievant Medsystems, Sunnyvale CA, US |
| Decision | Substantially Equivalent, May 3, 2019 |
| Received | Mar 1, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190504
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.