da Vinci Si Single-Site Instruments and Accessories, da Vinci Xi Single-Site Instruments and Accessories
K-Number: K170875 · 2017-09-12
Device Summary
Frequently Asked Questions
What is the da Vinci Si Single-Site Instruments and Accessories, da Vinci Xi Single-Site Instruments and Accessories?
da Vinci Si Single-Site Instruments and Accessories, da Vinci Xi Single-Site Instruments and Accessories is a medical device that received FDA 510(k) clearance on 2017-09-12. It is manufactured by Intuitive Surgical, Inc.. The 510(k) number is K170875.
When was da Vinci Si Single-Site Instruments and Accessories, da Vinci Xi Single-Site Instruments and Accessories approved by the FDA?
da Vinci Si Single-Site Instruments and Accessories, da Vinci Xi Single-Site Instruments and Accessories received FDA 510(k) clearance on 2017-09-12, under approval number K170875.
What company makes da Vinci Si Single-Site Instruments and Accessories, da Vinci Xi Single-Site Instruments and Accessories?
da Vinci Si Single-Site Instruments and Accessories, da Vinci Xi Single-Site Instruments and Accessories is manufactured by Intuitive Surgical, Inc..
What is the FDA product code for da Vinci Si Single-Site Instruments and Accessories, da Vinci Xi Single-Site Instruments and Accessories?
The FDA product code for da Vinci Si Single-Site Instruments and Accessories, da Vinci Xi Single-Site Instruments and Accessories is NAY.
Related Clinical Trials
Other Devices by Intuitive Surgical, Inc.
Related Devices (Code: NAY)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.