Novapproach Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novapproach Spine - FDA 510(k) Cleared Devices
Recent clearances: OneLIF Intervertebral Body Replacement System
1
Total
1
Cleared
0
Denied
Novapproach Spine has 1 FDA 510(k) cleared medical devices. Based in Alachua, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Novapproach 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 - Novapproach Spine
1 devices