CrossRoads Modular Tray System
K-Number: K241050 · 2024-07-16
Device Summary
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. The listed applicant is Crossroads Extremity Systems. The 510(k) number is K241050.
When did CrossRoads Modular Tray System receive FDA 510(k) clearance?
CrossRoads Modular Tray System received FDA 510(k) clearance on 2024-07-16, under 510(k) number K241050.
Who is the listed applicant for CrossRoads Modular Tray System?
The FDA 510(k) record lists Crossroads Extremity Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CrossRoads Modular Tray System?
The FDA product code for CrossRoads Modular Tray System is KCT.
Other records listing Crossroads Extremity Systems as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KCT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.