Bright Spine - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Bright Spine has 2 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Last cleared in 2023. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Bright Spine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lighthouse Regulatory Consulting Group as regulatory consultant.
2 devices