meddevicedb.com FDA Device Reference

HANAROSTENT Esophagus TTS (CCC), HANAROSTENT Esophagus TTS (NCN)

K200860 Class II Traditional
Decision Date
2020-05-20
Sponsor / Applicant
M.I.Tech Co., Ltd.

Technical Specification

510(k) Submission ID K200860
Product Code ESW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3610
Decision Date 2020-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HANAROSTENT Esophagus TTS (CCC), HANAROSTENT Esophagus TTS (NCN) received FDA 510(k) clearance under submission number K200860, sponsored by M.I.Tech Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2020-05-20.

Classification & Regulation

This clearance is catalogued under FDA product code ESW and 21 CFR 878.3610, within the General, Plastic Surgery review panel as a Class II device.