Medical Device Manufacturer · US , Newport Beach , CA

Apollo Spine, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2009

Recent clearances: VENUS FACET SCREW SYSTEM, ZENITH PEDICLE SYSTEM, ECLIPSE VERTEBRAL SPACER SYSTEM-LUMBAR

View 6 510(k) Devices ↓
6
Total
6
Cleared
0
Denied

FDA 510(k) Regulatory Record - Apollo Spine, Inc. Orthopedic ✕

6 devices
1-6 of 6
Cleared Oct 19, 2012
VENUS FACET SCREW SYSTEM
K120340 · MRW
Orthopedic · 259d
Cleared Mar 03, 2011
ZENITH PEDICLE SYSTEM
K102636 · MNH
Orthopedic · 171d
Cleared Jan 12, 2011
ECLIPSE VERTEBRAL SPACER SYSTEM-LUMBAR
K102121 · OVD
Orthopedic · 167d
Cleared Jan 07, 2011
ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICAL
K101588 · OVE
Orthopedic · 214d
Cleared Oct 23, 2009
COMET ANTERIOR CERVICAL PLATE SYSTEM
K090751 · KWQ
Orthopedic · 217d
Cleared Jan 27, 2009
APOLLO ANTERIOR CERVICAL PLATE SYSTEM
K082504 · KWQ
Orthopedic · 151d
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