Agile Esophageal OTW Stent System

FDA 510(k) K211960 · Boston Scientific Corporation

Substantially Equivalent

510(k) numberK211960

Submission

Device name
Agile Esophageal OTW Stent System
Applicant
Boston Scientific Corporation
Marlboro, MA, US
Received
June 24, 2021
Decision date
November 22, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ESW – Prosthesis, Esophageal
Device class
Class II (moderate risk)
Regulation
21 CFR 878.3610
Specialty
General, Plastic Surgery
Implant
Yes

Other 510(k)s with product code ESW

510(k)DeviceApplicantDecision
K261978WallFlex Esophageal Stent System;Agile Esophageal Over-the-Wire (OTW) Stent SystemESW · Special Boston Scientific Corporation07/10/2026SE
K253327HANAROSTENT Esophagus Upper (CCC)ESW · Special M.I.Tech Co., Ltd.10/30/2025SE
K243619Niti-S Esophageal Stent; Esophageal TTS StentESW · Traditional Taewoong Medical Co., Ltd.10/30/2025SE
K251265Resilience Fully Covered Esophageal Stent SystemESW · Traditional Merit Medical Systems, Inc.07/23/2025SE
K233939Ultraflex Esophageal NG Stent System; WallFlex Esophageal Stent SystemESW · Traditional Boston Scientific04/29/2024SE
K233837Agile Esophageal Stent SystemESW · Traditional Boston Scientific Corporation04/04/2024SE
K240522Esophageal TTS StentESW · Special Taewoong Medical03/22/2024SE
K223266Hilzo Esophageal StentsESW · Traditional Thoracent, Inc.01/16/2024SE
K221482Esophageal TTS StentESW · Special Taewoong Medical Co., Ltd.06/22/2022SE
K213251HANAROSTENT Esophagus Asymmetric (CCC)ESW · Special M.I.Tech Co., Ltd.11/18/2021SE

More from M.I.Tech Co., Ltd.

510(k)DeviceDecision
K262151SpaceOAR Flex™ SystemOVB · Traditional 09/11/2026SE
K262460Rezum SystemKNS · Traditional 09/03/2026SE
K261153LithoVue Elite Digital Flexible Ureteroscope SystemFGB · Traditional 08/26/2026SE
K253692AVVIGO™+ Multi-Modality Guidance SystemDQK · Traditional 08/21/2026SE
K262406EluPro Antibiotic-Eluting BioEnvelopeFTM · Special 08/12/2026SE
K261915Navigator™ Flex Ureteral Access Sheath SetFED · Traditional 08/04/2026SE
K262462TheraSphere 360™ Y-90 Management PlatformLLZ · Special 07/24/2026SE
K262165FARADRIVE™ Steerable Sheath (M004PF21M402)DRA · Special 07/24/2026SE
K261488OBSIDIO Conformable EmbolicKRD · Traditional 07/24/2026SE
K261978WallFlex Esophageal Stent System;Agile Esophageal Over-the-Wire (OTW) Stent SystemESW · Special 07/10/2026SE

Questions and answers

When was Agile Esophageal OTW Stent System cleared by the FDA?

Agile Esophageal OTW Stent System (K211960) received a 510(k) decision of Substantially Equivalent on November 22, 2021, 151 days after the submission was received.

What is the product code of K211960?

The FDA product code is ESW – Prosthesis, Esophageal, a Class II (moderate risk) device regulated under 21 CFR 878.3610.