Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Apollo Spine with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 19, 2012: VENUS FACET SCREW SYSTEM.
| Date | Record | Source |
|---|---|---|
| Oct 19, 2012 | VENUS FACET SCREW SYSTEMK120340 · MRW | 510(k) clearances |
| Feb 16, 2012 | ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICALK120143 · ODP | 510(k) clearances |
| Mar 3, 2011 | ZENITH PEDICLE SYSTEMK102636 · MNH | 510(k) clearances |
| Jan 12, 2011 | ECLIPSE VERTEBRAL SPACER SYSTEM-LUMBARK102121 · OVD | 510(k) clearances |
| Jan 7, 2011 | ECLIPSE VERTEBRAL SPACER SYSTEM-CERVICALK101588 · OVE | 510(k) clearances |
| Oct 23, 2009 | COMET ANTERIOR CERVICAL PLATE SYSTEMK090751 · KWQ | 510(k) clearances |
| Jan 27, 2009 | APOLLO ANTERIOR CERVICAL PLATE SYSTEMK082504 · KWQ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
