Integrity Spine - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Integrity Spine has 2 FDA 510(k) cleared medical devices. Based in Austin, US.
Last cleared in 2023. Active since 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Integrity Spine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jalex Medical, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Integrity Spine
2 devices