510(k) K202752 ยท QJP Catheter, Percutaneous, Neurovasculature
AXS Vecta 46 Intermediate Catheter
| Applicant | Stryker Neurovascular, Fremont CA, US |
| Decision | Substantially Equivalent, Aug 27, 2021 |
| Received | Sep 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202752
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.