meddevicedb.com FDA Device Reference

ENDOSCOPIC PLICATION SYSTEM; EPS; PLICATOR

K071553 Class II Traditional
Decision Date
2007-09-18
Sponsor / Applicant
Ndo Surgical, Inc.

Technical Specification

510(k) Submission ID K071553
Product Code ODE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2007-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOSCOPIC PLICATION SYSTEM; EPS; PLICATOR received FDA 510(k) clearance under submission number K071553, sponsored by Ndo Surgical, 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 2007-09-18.

Classification & Regulation

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