Cardinal Spine, LLC is one of 18522 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardinal Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: C-VBR, STGC-LORDOTIC, STGC
4
Total
4
Cleared
0
Denied
Cardinal Spine, LLC has 4 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 4 cleared submissions from 2011 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Cardinal Spine, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cardinal Spine, LLC
4 devices