meddevicedb.com FDA Device Reference

FMX314 Surgical Platform

K160797 Class II Traditional
Decision Date
2016-08-26
Sponsor / Applicant
Fortimedix Surgical B.V.

Technical Specification

510(k) Submission ID K160797
Product Code OTJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2016-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FMX314 Surgical Platform received FDA 510(k) clearance under submission number K160797, sponsored by Fortimedix Surgical B.V.. 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 2016-08-26.

Classification & Regulation

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