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FDA 510(k)

X-Guide Surgical Navigation System

K-Number: K192579 · 2020-02-03

Decision Date2020-02-03
Product CodePLV
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

X-Guide Surgical Navigation System is a medical device manufactured by X-Nav Technologies, LLC. It received FDA 510(k) clearance on 2020-02-03 under approval number K192579. The device is classified under product code PLV. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-Guide Surgical Navigation System?

X-Guide Surgical Navigation System is a medical device that received FDA 510(k) clearance on 2020-02-03. It is manufactured by X-Nav Technologies, LLC. The 510(k) number is K192579.

When was X-Guide Surgical Navigation System approved by the FDA?

X-Guide Surgical Navigation System received FDA 510(k) clearance on 2020-02-03, under approval number K192579.

What company makes X-Guide Surgical Navigation System?

X-Guide Surgical Navigation System is manufactured by X-Nav Technologies, LLC.

What is the FDA product code for X-Guide Surgical Navigation System?

The FDA product code for X-Guide Surgical Navigation System is PLV.

Related Clinical Trials

Related PubMed Literature

Other Devices by X-Nav Technologies, 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.