510(k) K260130 ยท MOF Guide, Wire, Catheter, Neurovasculature
Willow 18 Guidewire
| Applicant | Arbor Endovascular, LLC, San Jose CA, US |
| Decision | Substantially Equivalent, Feb 13, 2026 |
| Received | Jan 16, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K260130
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.