510(k) K241050

CrossRoads Modular Tray System by Crossroads Extremity Systems — Product Code KCT

K241050 is an FDA 510(k) premarket notification submitted by Crossroads Extremity Systems for the device "CrossRoads Modular Tray System". The FDA issued a decision of Substantially Equivalent on July 16, 2024. The device falls under product code KCT (Sterilization Wrap Containers, Trays, Cassettes & Other Accessories), a Class II device regulated under 21 CFR 880.6850. Crossroads Extremity Systems has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 16, 2024
Date Received
April 17, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device Class
Class II
Regulation Number
880.6850
Review Panel
HO
Submission Type