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da Vinci Xi Surgical System, da Vinci X Surgical System

K191529 Class II Traditional
Decision Date
2020-02-06
Sponsor / Applicant
Intuitive Surgical

Technical Specification

510(k) Submission ID K191529
Product Code NAY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2020-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

da Vinci Xi Surgical System, da Vinci X Surgical System received FDA 510(k) clearance under submission number K191529, sponsored by Intuitive Surgical. 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 2020-02-06.

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.