Happe Spine - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Happe Spine has 1 FDA 510(k) cleared medical devices. Based in Grand Rapids, US.
Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Happe Spine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Happe Spine
1 devices