510(k) K261772 ยท HCG Device, Neurovascular Embolization
Target Xtra Detachable Coil
| Applicant | Stryker Neurovscular, Fremont CA, US |
| Decision | Substantially Equivalent, Jun 24, 2026 |
| Received | May 29, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261772
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.