meddevicedb.com FDA Device Reference

SimpleStitch Suturing System

K243750 Class II Traditional
Decision Date
2025-04-17
Sponsor / Applicant
Envision Endoscopy

Technical Specification

510(k) Submission ID K243750
Product Code OCW
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2025-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SimpleStitch Suturing System received FDA 510(k) clearance under submission number K243750, sponsored by Envision Endoscopy. 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 2025-04-17.

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.