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FDA 510(k)

G Surgical Marksman System

K-Number: K193219 · 2019-12-17

Decision Date2019-12-17
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

G Surgical Marksman System is the device name listed in this FDA 510(k) record. The listed applicant is G Surgical, LLC. It received FDA 510(k) clearance on 2019-12-17 under 510(k) number K193219. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G Surgical Marksman System?

G Surgical Marksman System is a medical device that received FDA 510(k) clearance on 2019-12-17. The listed applicant is G Surgical, LLC. The 510(k) number is K193219.

When did G Surgical Marksman System receive FDA 510(k) clearance?

G Surgical Marksman System received FDA 510(k) clearance on 2019-12-17, under 510(k) number K193219.

Who is the listed applicant for G Surgical Marksman System?

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

What is the FDA product code for G Surgical Marksman System?

The FDA product code for G Surgical Marksman System is NKB.

Other records listing G Surgical, LLC 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.

Related Devices (Code: NKB)

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

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