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510k Database
Manufacturers
US
Spinecraft, Inc.
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Medical Device Manufacturer
·
US , Westchester , IL
Spinecraft, Inc. - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 2006
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Spinecraft, Inc.
Orthopedic
✕
3
devices
1-3 of 3
Filters
Cleared
Mar 16, 2010
APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHER
K092825
·
KWP
Orthopedic
·
186d
Cleared
Dec 22, 2006
APEX SPINE SYSTEM
K062513
·
KWP
Orthopedic
·
116d
Cleared
Oct 19, 2006
OSTEOPORE TCP
K062496
·
MQV
Orthopedic
·
55d
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Orthopedic
3