K260537
- 510(k) number
- K260537
- Device name
- Willow 24 Guidewire
- Applicant
- Arbor Endovascular, LLC CA · US
- Product code
- MOF — Guide, Wire, Catheter, Neurovasculature
- Decision date
- 2026-03-19
- Date received
- 2026-02-17
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K260537.pdf
Official FDA record: K260537
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.