Medical Device Manufacturer · US , American Fork , UT

Sanacor - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2007
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Sanacor Orthopedic ✕

3 devices
1-3 of 3
Cleared Jul 27, 2009
ALPINE PEDICLE SCREW SYSTEM
K090477 · MNH
Orthopedic · 153d
Cleared Jul 03, 2008
ACTIVE ANTERIOR CERVICAL PLATE SYSTEM
K073500 · KWQ
Orthopedic · 203d
Cleared Jun 13, 2007
LOWTOP PEDICLE SCREW SYSTEM
K070933 · MNH
Orthopedic · 71d
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