meddevicedb.com FDA Device Reference

Senhance Surgical System

K202166 Class II Traditional
Decision Date
2021-03-02
Sponsor / Applicant
Transenterix, Inc.

Technical Specification

510(k) Submission ID K202166
Product Code NAY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2021-03-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Senhance Surgical System received FDA 510(k) clearance under submission number K202166, sponsored by Transenterix, 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 2021-03-02.

Classification & Regulation

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