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 15, 2026, FDA's public records list Camber Spine Technologies with 23 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 2024: SPIRA® Anterior Lumbar Spacers.
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.
| Jul 12, 2024 | SPIRA® Anterior Lumbar SpacersK234077 · MAX | 510(k) clearances |
| Apr 16, 2024 | Alcantara Thoracolumbar Plate SystemK232256 · KWQ | 510(k) clearances |
| Feb 27, 2024 | Camber Sacroiliac (SI) Fixation SystemK233972 · OUR | 510(k) clearances |
| Jul 11, 2023 | SPIRA® Posterior Lumbar SpacersK230942 · MAX | 510(k) clearances |
| Mar 30, 2023 | ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)K221324 · OVD | 510(k) clearances |
| Mar 22, 2023 | SPIRA®-C Integrated Fixation SystemK223837 · OVE | 510(k) clearances |
| Sep 2, 2022 | Camber Sacroiliac (SI) Fixation SystemK203503 · OUR | 510(k) clearances |
| Apr 29, 2022 | Camber Spine Navigation SystemK220038 · OLO | 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
