Medical Device Manufacturer · US , Alameda , CA

Spartek Medical, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010

Recent clearances: SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM, SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM

View 2 510(k) Devices ↓
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Spartek Medical, Inc. Orthopedic ✕

2 devices
1-2 of 2
Cleared Feb 17, 2011
SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM
K103383 · NKB
Orthopedic · 91d
Cleared May 07, 2010
SPARTEK VARIABLE ANGLE PEDICLE SCREW POSTERIOR FUSION SYSTEM
K094002 · NKB
Orthopedic · 130d
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