Apollo Spine, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K120340 | VENUS FACET SCREW SYSTEM | MRW | 2012-10-19 | View |
| 510(k) | K102636 | ZENITH PEDICLE SYSTEM | MNH | 2011-03-03 | View |
| 510(k) | K102121 | ECLIPSE VERTEBRAL SPACER SYSTEM-LUMBAR | OVD | 2011-01-12 | View |
| 510(k) | K101588 | ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICAL | OVE | 2011-01-07 | View |
| 510(k) | K090751 | COMET ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2009-10-23 | View |
| 510(k) | K082504 | APOLLO ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2009-01-27 | View |
No matching devices.
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