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 15, 2026, FDA's public records list Advanced Spine Fixation Systems with 16 510(k) clearances. The most recent is a 510(k) clearance dated Feb 4, 2000: WILTSE SYSTEM.
| Feb 4, 2000 | WILTSE SYSTEMK992012 · KWQ | 510(k) clearances |
| Apr 13, 1999 | MODIFICATION TO PARTS NUMBERED CGT-SL AND CGT-SL-15K990845 · KWP | 510(k) clearances |
| Jan 25, 1996 | CENTRA-LINE GRAPPLE, VARIFIX SYSTEMK954770 · KWP | 510(k) clearances |
| Nov 7, 1995 | SADDLE WITH ANCHOR, STAINLESS STEEL VARIFIX SYSTEMK953779 · MNH | 510(k) clearances |
| Nov 6, 1995 | SADDLE WITH ANCHOR, TITANIUM VARIFIX SYSTEMK953778 · MNH | 510(k) clearances |
| Sep 8, 1995 | STAINLESS STEEL VARIFIX SYSTEM 5.0MM DIAMETER ANCHOR SCREWK953369 · MNH | 510(k) clearances |
| Jul 26, 1995 | 5.8MM DIAMETER ANCHOR SCREWK951308 · MNH | 510(k) clearances |
| Jul 25, 1995 | TITANIUM LOW PROFILE CROSS BARK951172 · 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
