RecallHawk

WallFlex Colonic Stent System with Anchor Lock Delivery System; WallFlex Duodenal Stent System with Anchor Lock Delivery

Boston Scientific Corporation

Summary

Boston Scientific Corporation received 510(k) clearance for 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, a MQR device. Cleared on 2024-03-08.

Details

Source

510(k) Clearance

External ID

K234046

Action Date

2024-03-08

Status

Special

Category

device

Product Code

MQR

Product Description

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. Product code: MQR.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 413 device clearances issued this month. Boston Scientific Corporation has received 65 total clearances in our database.

Boston Scientific Corporation has 399 FDA actions in our database, including 334 recalls and 65 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Boston Scientific Corporation have FDA actions?

Boston Scientific Corporation has 399 FDA actions in our database, including 334 recalls and 65 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K234046" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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