Depuy Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Depuy Spine - FDA 510(k) Cleared Devices
Recent clearances: CONDUIT Cages
3
Total
3
Cleared
0
Denied
Depuy Spine has 3 FDA 510(k) cleared medical devices. Based in Raynham, US.
Last cleared in 2022. Active since 2008. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Depuy Spine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Depuy Spine
3 devices