Clearance Summary
WallFlex Biliary RX Fully Covered Stent System RMV received FDA 510(k) clearance under submission number DEN150040, sponsored by Boston Scientific. The device was reviewed via the Direct premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2016-06-03.
- Submission: DEN150040
- Applicant / Sponsor: Boston Scientific
- Clearance pathway: Direct
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5011
- Decision date: 2016-06-03
Classification & Regulation
This clearance is catalogued under FDA product code PNB and 21 CFR 876.5011, within the Gastroenterology, Urology review panel as a Class II device.