510(k) K243593 ยท QJP Catheter, Percutaneous, Neurovasculature
AXS Lift Intracranial Base Catheter
| Applicant | Stryker Neurovascular, Fremont CA, US |
| Decision | Substantially Equivalent, Feb 18, 2025 |
| Received | Nov 20, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243593
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.