X-Guide Surgical Navigation System
K-Number: K192579 · 2020-02-03
Device Summary
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
Related Devices (Code: PLV)
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.