Cit Ortho is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cit Ortho - FDA 510(k) Cleared Devices
Recent clearances: C Scope Visualization System
1
Total
1
Cleared
0
Denied
Cit Ortho has 1 FDA 510(k) cleared medical devices. Based in Westlake, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Cit Ortho Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cit Ortho
1 devices