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 14, 2026, FDA's public records list RSB Spine with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jan 27, 2010: C-PS PEEK OPTIMA CERVICAL INTERBODY SPACER, L-PS PEEK OPTIMA LUMBAR INTERBODY SPACER.
| Jan 27, 2010 | C-PS PEEK OPTIMA CERVICAL INTERBODY SPACER, L-PS PEEK OPTIMA LUMBAR INTERBODY SPACERK092540 · ODP | 510(k) clearances |
| Oct 6, 2009 | INTERPLATE CK092070 · KWQ | 510(k) clearances |
| May 29, 2008 | INTERPLATE PEEK CERVICAL INTERBODY FUSION DEVICE (IFD)K081194 · OVE | 510(k) clearances |
| Sep 18, 2007 | INTERPLATE INTERBODY FUSION DEVICE, MODELS C, CGC, L AND LGCK071922 · OVD | 510(k) clearances |
| Jun 11, 2007 | MODIFICATION TO: INTERPLATE VBR SYSTEMK071372 · MQP | 510(k) clearances |
| Apr 19, 2007 | INTERPLATE VBR SYSTEMK070316 · MQP | 510(k) clearances |
| Aug 18, 2006 | INTERPLATE VBR SYSTEMK061401 · MQP | 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
