Medical device makerLabelled 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 Spinal USA with 24 510(k) clearances. The most recent is a 510(k) clearance dated Nov 25, 2013: VAULT-C INTERVERTEBRAL BODY FUSION DEVICE.
| Nov 25, 2013 | VAULT-C INTERVERTEBRAL BODY FUSION DEVICEK132029 · OVE | 510(k) clearances |
| Aug 9, 2013 | FACET SCREW SYSTEMK130863 · MRW | 510(k) clearances |
| Jul 24, 2013 | REFORM PEDICLE SCREW SYSTEMK131343 · MNI | 510(k) clearances |
| Jun 20, 2013 | REFORM PEDICLE SCREW SYSTEMK130279 · MNI | 510(k) clearances |
| Apr 25, 2013 | VAULT ALIF SYSTEMK130445 · OVD | 510(k) clearances |
| Nov 20, 2012 | S-LOK PSS SYSTEMK122931 · MNI | 510(k) clearances |
| Aug 8, 2012 | REFORM PEDICLE SCREW SYSTEMK121172 · MNI | 510(k) clearances |
| Jul 11, 2012 | SLIMPLICITY SOLO ANTERIOR CERVICAL PLATE SYSTEMK112748 · 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
