meddevicedb.com FDA Device Reference

OverStitch NXT Endoscopic Suturing System

K231553 Class II Special
Decision Date
2023-06-29
Sponsor / Applicant
Apollo Endosurgery, Inc.

Technical Specification

510(k) Submission ID K231553
Product Code OCW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2023-06-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OverStitch NXT Endoscopic Suturing System received FDA 510(k) clearance under submission number K231553, sponsored by Apollo Endosurgery, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2023-06-29.

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.