Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Intuitive Surgical EndoWrist Vessel Sealer Extend

K-Number: K173337 · 2018-04-26

Decision Date2018-04-26
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Intuitive Surgical EndoWrist Vessel Sealer Extend is the device name listed in this FDA 510(k) record. The listed applicant is Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2018-04-26 under 510(k) number K173337. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intuitive Surgical EndoWrist Vessel Sealer Extend?

Intuitive Surgical EndoWrist Vessel Sealer Extend is a medical device that received FDA 510(k) clearance on 2018-04-26. The listed applicant is Intuitive Surgical, Inc.. The 510(k) number is K173337.

When did Intuitive Surgical EndoWrist Vessel Sealer Extend receive FDA 510(k) clearance?

Intuitive Surgical EndoWrist Vessel Sealer Extend received FDA 510(k) clearance on 2018-04-26, under 510(k) number K173337.

Who is the listed applicant for Intuitive Surgical EndoWrist Vessel Sealer Extend?

The FDA 510(k) record lists Intuitive Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intuitive Surgical EndoWrist Vessel Sealer Extend?

The FDA product code for Intuitive Surgical EndoWrist Vessel Sealer Extend is NAY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Intuitive Surgical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 124 devices →

Related Devices (Code: NAY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.