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FDA 510(k)

CrossRoads Modular Tray System

K-Number: K241050 · 2024-07-16

Decision Date2024-07-16
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CrossRoads Modular Tray System is a medical device manufactured by Crossroads Extremity Systems. It received FDA 510(k) clearance on 2024-07-16 under approval number K241050. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CrossRoads Modular Tray System?

CrossRoads Modular Tray System is a medical device that received FDA 510(k) clearance on 2024-07-16. It is manufactured by Crossroads Extremity Systems. The 510(k) number is K241050.

When was CrossRoads Modular Tray System approved by the FDA?

CrossRoads Modular Tray System received FDA 510(k) clearance on 2024-07-16, under approval number K241050.

What company makes CrossRoads Modular Tray System?

CrossRoads Modular Tray System is manufactured by Crossroads Extremity Systems.

What is the FDA product code for CrossRoads Modular Tray System?

The FDA product code for CrossRoads Modular Tray System is KCT.

Related Clinical Trials

Other Devices by Crossroads Extremity Systems

Related Devices (Code: KCT)

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.