Crossroads Extremity Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Crossroads Extremity Systems - FDA 510(k) Cleared Devices
Recent clearances: TRILEAP Plating System, CrossRoads Modular Tray System, TriLEAP Plating System
3
Total
3
Cleared
0
Denied
Crossroads Extremity Systems has 3 FDA 510(k) cleared medical devices. Based in Memphis, US.
Latest FDA clearance: Jan 2026. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Crossroads Extremity Systems Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Crossroads Extremity Systems
3 devices