Medical Device Manufacturer · US , Apple Valley , MN

Spineselect, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008

Recent clearances: SPINESELECT POLYSCREW PEDICLE SCREW SYSTEM, TURBO PRIME IBD SYSTEM

View 2 510(k) Devices ↓
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Spineselect, LLC Orthopedic ✕

2 devices
1-2 of 2
Cleared Jan 13, 2014
SPINESELECT POLYSCREW PEDICLE SCREW SYSTEM
K133066 · NKB
Orthopedic · 108d
Cleared Apr 16, 2008
TURBO PRIME IBD SYSTEM
K080058 · MAX
Orthopedic · 98d
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