Medical Device Manufacturer · US , Brandon , MS

Spinal USA - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 2006
23
Total
23
Cleared
0
Denied

Spinal USA has 23 FDA 510(k) cleared orthopedic devices. Based in Brandon, US.

Historical record: 23 cleared submissions from 2006 to 2013.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Spinal USA
23 devices
1-12 of 23
Cleared Nov 25, 2013
VAULT-C INTERVERTEBRAL BODY FUSION DEVICE
K132029 · OVE
Orthopedic · 147d
Cleared Aug 09, 2013
FACET SCREW SYSTEM
K130863 · MRW
Orthopedic · 134d
Cleared Jul 24, 2013
REFORM PEDICLE SCREW SYSTEM
K131343 · MNI
Orthopedic · 76d
Cleared Jun 20, 2013
REFORM PEDICLE SCREW SYSTEM
K130279 · MNI
Orthopedic · 135d
Cleared Apr 25, 2013
VAULT ALIF SYSTEM
K130445 · OVD
Orthopedic · 63d
Cleared Nov 20, 2012
S-LOK PSS SYSTEM
K122931 · MNI
Orthopedic · 57d
Cleared Aug 08, 2012
REFORM PEDICLE SCREW SYSTEM
K121172 · MNI
Orthopedic · 113d
Cleared Sep 15, 2011
SURE LOK MINI POSTERIOR CERVICAL/UPPER THORACIC SYSTEM
K112025 · KWP
Orthopedic · 62d
Cleared Apr 04, 2011
VAULT ALIF SYSTEM
K103369 · OVD
Orthopedic · 138d
Cleared Nov 17, 2009
SPINAL USA RCS ANTERIOR LUMBAR BUTRESS PLATE SYSTEM, MODEL 22-1001-25
K092659 · KWQ
Orthopedic · 81d
Cleared Sep 25, 2009
SPINAL USA INTERBODY CAGES
K092193 · MAX
Orthopedic · 66d
Cleared Sep 14, 2009
MODIFICATION TO: PSS SYSTEM
K092128 · MNI
Orthopedic · 61d
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