K242950
- 510(k) number
- K242950
- Device name
- WallFlex Biliary PLUS RX Stent System
- Applicant
- Boston Scientific MA · US
- Product code
- FGE — Stents, Drains And Dilators For The Biliary Ducts
- Decision date
- 2024-12-06
- Date received
- 2024-09-23
- Decision
- Unknown
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K242950.pdf
Official FDA record: K242950
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.