510(k) K261866 · KRD Device, Vascular, For Promoting Embolization
Concerto Versa Detachable Coil
| Applicant | Medtronic, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Jun 24, 2026 |
| Received | Jun 4, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261866
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.