meddevicedb.com FDA Device Reference

X-Tack Endoscopic HeliX Tacking System

K201808 Class II Traditional
Decision Date
2020-12-15
Sponsor / Applicant
Apollo Endosurgery, Inc.

Technical Specification

510(k) Submission ID K201808
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 2020-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

X-Tack Endoscopic HeliX Tacking System received FDA 510(k) clearance under submission number K201808, 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 2020-12-15.

Classification & Regulation

This clearance is catalogued under FDA product code PKL and 21 CFR 876.4400, within the Gastroenterology, Urology review panel as a Class II device.