WallFlex Colonic Stent System with Anchor Lock Delivery System
K-Number: K201159 · 2020-08-17
Device Summary
Frequently Asked Questions
What is the WallFlex Colonic Stent System with Anchor Lock Delivery System?
WallFlex Colonic Stent System with Anchor Lock Delivery System is a medical device that received FDA 510(k) clearance on 2020-08-17. The listed applicant is Boston Scientific Corporation. The 510(k) number is K201159.
When did WallFlex Colonic Stent System with Anchor Lock Delivery System receive FDA 510(k) clearance?
WallFlex Colonic Stent System with Anchor Lock Delivery System received FDA 510(k) clearance on 2020-08-17, under 510(k) number K201159.
Who is the listed applicant for WallFlex Colonic Stent System with Anchor Lock Delivery System?
The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WallFlex Colonic Stent System with Anchor Lock Delivery System?
The FDA product code for WallFlex Colonic Stent System with Anchor Lock Delivery System is MQR.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Boston Scientific Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MQR)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.