Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Spectrum Spine with 8 510(k) clearances. The most recent is a 510(k) clearance dated Mar 30, 2026: Spectrum Spine Cervical Cage System; Spectrum Spine Lumbar Cage System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 30, 2026 | Spectrum Spine Cervical Cage System; Spectrum Spine Lumbar Cage SystemK252240 · ODP | 510(k) clearances |
| Oct 24, 2025 | Expandable Titanium PLIF/TLIF SystemK253377 · MAX | 510(k) clearances |
| Apr 4, 2025 | Spectrum Spine Lumbar Cage SystemK243074 · MAX | 510(k) clearances |
| May 30, 2024 | Spectrum Spine Cervical Cage SystemK240838 · ODP | 510(k) clearances |
| Apr 29, 2021 | Expandable Titanium PLIF/TLIF SystemK201024 · MAX | 510(k) clearances |
| Mar 7, 2019 | Spectrum Spine Expandable Cages (SSEC)K173518 · MAX | 510(k) clearances |
| Oct 28, 2013 | SPECTRUM SPINE FENESTRATED FACET SCREW SYSTEMK132126 · MRW | 510(k) clearances |
| Feb 7, 2013 | SPECTRUM SPINE LAMINOPLASTY PLATING SYSTEMK122822 · NQW | 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
