Clearance Summary
WallFlex Colonic Stent System with Anchor Lock Delivery System; WallFlex Duodenal Stent System with Anchor Lock Delivery System; WallFlex Colonic Soft Stent System with Anchor Lock Delivery System; WallFlex Duodenal Soft Stent System with Anchor Lock Delivery System received FDA 510(k) clearance under submission number K234046, sponsored by Boston Scientific Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-03-08.
- Submission: K234046
- Applicant / Sponsor: Boston Scientific Corporation
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3610
- Decision date: 2024-03-08
Classification & Regulation
This clearance is catalogued under FDA product code MQR and 21 CFR 878.3610, within the General, Plastic Surgery review panel as a Class II device.