Medical Device Manufacturer · US , Sunnyvale , CA

Medtronic Spine, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010
2
Total
2
Cleared
0
Denied

Medtronic Spine, LLC has 2 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Medtronic Spine, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medtronic Spine, LLC
2 devices
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