Crossroads Extemity Systems, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Crossroads Extemity Systems, LLC - FDA 510(k) Cleared Devices
Recent clearances: MotoBAND CP Implant System, CrossRoads Screw System, TriMAX Implant System
3
Total
3
Cleared
0
Denied
Crossroads Extemity Systems, LLC has 3 FDA 510(k) cleared medical devices. Based in Memphis, US.
Historical record: 3 cleared submissions from 2019 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Crossroads Extemity Systems, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mrc X, LLC and Mrc-X, LLC.
FDA 510(k) Regulatory Record - Crossroads Extemity Systems, LLC
3 devices