Medical Device Manufacturer · US , Apple Valley , MN

Spinal Devices, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009
2
Total
2
Cleared
0
Denied

Spinal Devices, LLC has 2 FDA 510(k) cleared medical devices. Based in Apple Valley, US.

Historical record: 2 cleared submissions from 2009 to 2009. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Spinal Devices, LLC
2 devices
1-2 of 2
Cleared Feb 27, 2009
TIGER DISCECTOMY DEVICE
K081240 · HRX
Orthopedic · 302d
Cleared Jan 13, 2009
PHENIX CERVICAL INTERBODY DEVICE
K083167 · ODP
Orthopedic · 78d
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