510(k) K170987 ยท MMX Device, Percutaneous Retrieval
Captus Vascular Retrieval System
| Applicant | Avantec Vascular Corporation, Sunnyvale CA, US |
| Decision | Substantially Equivalent, Aug 28, 2017 |
| Received | Apr 3, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170987
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.