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FDA 510(k)

Orthoscan TAU MVP Mini C-Arm System

K-Number: K252579 · 2026-01-14

Decision Date2026-01-14
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Orthoscan TAU MVP Mini C-Arm System is a medical device manufactured by Ziehm-Orthoscan, Inc.. It received FDA 510(k) clearance on 2026-01-14 under approval number K252579. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Orthoscan TAU MVP Mini C-Arm System?

Orthoscan TAU MVP Mini C-Arm System is a medical device that received FDA 510(k) clearance on 2026-01-14. It is manufactured by Ziehm-Orthoscan, Inc.. The 510(k) number is K252579.

When was Orthoscan TAU MVP Mini C-Arm System approved by the FDA?

Orthoscan TAU MVP Mini C-Arm System received FDA 510(k) clearance on 2026-01-14, under approval number K252579.

What company makes Orthoscan TAU MVP Mini C-Arm System?

Orthoscan TAU MVP Mini C-Arm System is manufactured by Ziehm-Orthoscan, Inc..

What is the FDA product code for Orthoscan TAU MVP Mini C-Arm System?

The FDA product code for Orthoscan TAU MVP Mini C-Arm System is OXO.

Other Devices by Ziehm-Orthoscan, Inc.

Related Devices (Code: OXO)

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.