Medical Device Manufacturer · US , Encino , CA

Core-Nexus - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Core-Nexus Orthopedic ✕
2 devices
1-2 of 2
Cleared Aug 09, 2013
CORE PEDICLE SCREW SYSTEM
K131522 · MNI
Orthopedic · 73d
Cleared Jul 11, 2013
NEXUS ANTERIOR CERVICAL PLATE SYSTEM
K131520 · KWQ
Orthopedic · 44d
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