Depuy Synthes Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Depuy Synthes Spine - FDA 510(k) Cleared Devices
Recent clearances: SYNMESH System, DePuy Synthes T-PAL Spacer System
2
Total
2
Cleared
0
Denied
Depuy Synthes Spine has 2 FDA 510(k) cleared medical devices. Based in Raynham, US.
Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Depuy Synthes Spine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DePuy Synthes as regulatory consultant.
FDA 510(k) Regulatory Record - Depuy Synthes Spine
2 devices