K260938
- 510(k) number
- K260938
- Device name
- PATH BGC
- Applicant
- Crossroads Neurovascular, Inc. CA · US
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2026-04-15
- Date received
- 2026-03-20
- 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: K260938.pdf
Official FDA record: K260938
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.