Medical Device Manufacturer · US , Raynham , MA

Depuy Spine - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2008
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
1-3 of 3
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All3 Orthopedic 3