510(k) K222533 ยท HCG Device, Neurovascular Embolization
Target Tetra Detachable Coils
| Applicant | Stryker Neurovascular, Fremont CA, US |
| Decision | Substantially Equivalent, Dec 14, 2022 |
| Received | Aug 22, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222533
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.