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 its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list US Spine with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 22, 2008: PHANTOM PLUS CAGE SYSTEM.
| Dec 22, 2008 | PHANTOM PLUS CAGE SYSTEMK082801 · ODP | 510(k) clearances |
| Sep 24, 2008 | MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEMK081883 · MNH | 510(k) clearances |
| Jun 6, 2008 | PREFERENCE PEDICLE SCREW SYSTEMK081296 · MNH | 510(k) clearances |
| Dec 26, 2006 | LTD POLYAXIAL FIXATION SYSTEMK062785 · KWP | 510(k) clearances |
| Jun 19, 2006 | US SPINE FACET FIXATION SYSTEMK061041 · MRW | 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
