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 Spine View with 9 510(k) clearances. The most recent is a 510(k) clearance dated Aug 1, 2016: SpineView X-Pac Expandable Lumbar Cage System.
| Date | Record | Source |
|---|---|---|
| Aug 1, 2016 | SpineView X-Pac Expandable Lumbar Cage SystemK160856 · MAX | 510(k) clearances |
| Feb 24, 2016 | SpineView X-Pac Expandable Lumbar Cage SystemK152539 · MAX | 510(k) clearances |
| Dec 27, 2012 | FLEXLITE CAMERAK122134 · HRX | 510(k) clearances |
| Aug 16, 2012 | SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS)K121548 · HRX | 510(k) clearances |
| Jun 26, 2012 | ENSPIRE DISCECTOMY SYSTEMK120680 · HRX | 510(k) clearances |
| Feb 10, 2012 | SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS)K113362 · HRX | 510(k) clearances |
| Oct 21, 2011 | ENSPIRE DEBRIDER SYSTEMK110992 · HRX | 510(k) clearances |
| Apr 15, 2009 | ENSPIRE DEBRIDER SYSTEMK090278 · HRX | 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
