Cleared Traditional

Elastic Traction System

K222354 · Micro-Tech (Nanjing) Co., Ltd. · Gastroenterology & Urology
Oct 2022
Decision
60d
Days
Class 2
Risk

About This 510(k) Submission

K222354 is an FDA 510(k) clearance for the Elastic Traction System, a Endoscopic Traction Device (Class II — Special Controls, product code QSW), submitted by Micro-Tech (Nanjing) Co., Ltd. (Nanjing, CN). The FDA issued a Cleared decision on October 3, 2022, 60 days after receiving the submission on August 4, 2022. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.4410.

Submission Details

510(k) Number K222354 FDA.gov
FDA Decision Cleared SESE
Date Received August 04, 2022
Decision Date October 03, 2022
Days to Decision 60 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code QSW — Endoscopic Traction Device
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.4410
Definition An Endoscopic Traction Device Is A Prescription Device That Is Endoscopically Applied To Retract Tissue In The Gastrointestinal Tract During Dissection Procedures To Increase Visualization Of The Dissection Plane And Assist In Tissue Resection, Exposure, And Removal.