510(k) K213836 ยท GXI Probe, Radiofrequency Lesion
Intracept Intraosseous Nerve Ablation System
| Applicant | Relievant Medsystems, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Mar 11, 2022 |
| Received | Dec 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213836
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.