K253168
- 510(k) number
- K253168
- Device name
- 0.014 Willow Guidewire
- Applicant
- Arbor Endovascular, LLC CA · US
- Product code
- MOF — Guide, Wire, Catheter, Neurovasculature
- Decision date
- 2025-11-26
- Date received
- 2025-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K253168.pdf
Official FDA record: K253168
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.