meddevicedb.com FDA Device Reference

OverStitch SX Endoscopic Suturing System (ESS)

K171886 Class II Traditional
Decision Date
2017-11-15
Sponsor / Applicant
Apollo Endosurgery, Inc.

Technical Specification

510(k) Submission ID K171886
Product Code OCW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2017-11-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OverStitch SX Endoscopic Suturing System (ESS) received FDA 510(k) clearance under submission number K171886, sponsored by Apollo Endosurgery, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2017-11-15.

Classification & Regulation

This clearance is catalogued under FDA product code OCW and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.