510(k) K241768 ยท QJP Catheter, Percutaneous, Neurovasculature
Broadway 8 Catheter
| Applicant | Stryker Neurovascular, Fremont CA, US |
| Decision | Substantially Equivalent, Dec 19, 2024 |
| Received | Jun 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241768
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.