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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 a medical device manufactured by G Surgical, LLC. It received FDA 510(k) clearance on 2019-12-17 under approval 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. It is manufactured by G Surgical, LLC. The 510(k) number is K193219.

When was G Surgical Marksman System approved by the FDA?

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

What company makes G Surgical Marksman System?

G Surgical Marksman System is manufactured by G Surgical, LLC.

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

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

Related Clinical Trials

Related PubMed Literature

Other Devices by G Surgical, LLC

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.