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Senhance Surgical System

K192877 Class II Special
Decision Date
2019-11-22
Sponsor / Applicant
Transenterix, Inc.

Technical Specification

510(k) Submission ID K192877
Product Code NAY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2019-11-22
Clearance Pathway Special

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 K192877, sponsored by Transenterix, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2019-11-22.

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.