K260223
- 510(k) number
- K260223
- Device name
- Aristotle Mini Guidewire
- Applicant
- Scientia Vascular, Inc. UT · US
- Product code
- MOF — Guide, Wire, Catheter, Neurovasculature
- Decision date
- 2026-08-06
- Date received
- 2026-01-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K260223.pdf
Official FDA record: K260223
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.