Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Vertebron with 11 510(k) clearances. The most recent is a 510(k) clearance dated Jul 3, 2008: VERTEBRON SSP CERVICAL PLATING SYSTEM.
| Date | Record | Source |
|---|---|---|
| Jul 3, 2008 | VERTEBRON SSP CERVICAL PLATING SYSTEMK081567 · KWQ | 510(k) clearances |
| Jul 2, 2008 | MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEMK081597 · MNI | 510(k) clearances |
| Mar 24, 2008 | VERTEBRON VBR SYSTEMK073502 · MQP | 510(k) clearances |
| Jun 13, 2007 | MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEMK071376 · NKB | 510(k) clearances |
| Aug 16, 2006 | VERTEBRON SCP CERVICAL PLATE SYSTEMK062110 · KWQ | 510(k) clearances |
| Oct 17, 2005 | MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEMK051815 · KWQ | 510(k) clearances |
| Sep 7, 2005 | VERTEBRON PSS PEDICLE SCREW SYSTEMK051716 · KWP | 510(k) clearances |
| Feb 1, 2005 | VERTEBRON PSS PEDICLE SCREW SYSTEMK043152 · MNH | 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
