Medical Device Manufacturer · US , Westmont , IL

SpineCraft - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2009
Official Website
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - SpineCraft Orthopedic ✕
3 devices
1-3 of 3
Cleared Apr 16, 2026
ORIO-3D Cage System
K253260 · ODP
Orthopedic · 199d
Cleared Mar 04, 2026
ANTERIS Thoracolumbar Plate System
K260015 · KWQ
Orthopedic · 58d
Cleared Oct 30, 2009
ORIO-C CERVICAL, ORIO-TL TLIF, ORIO-PL PLIF, ORIO-AL ALIF INTERVEDRTEBRAL...
K090887 · ODP
Orthopedic · 213d
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