510(k) K260337 · GXD Generator, Lesion, Radiofrequency
SEEG-Tx® System (STX-SYS-001)
| Applicant | Dixi Medical, Marchaux-Chaudefontaine, FR |
| Decision | Substantially Equivalent, Oct 29, 2026 |
| Received | Feb 2, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260337
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.