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 14, 2026, FDA's public records list Neurostructures with 19 510(k) clearances. The most recent is a 510(k) clearance dated Oct 2, 2020: Oculus-SA 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.
| Oct 2, 2020 | Oculus-SA Lumbar Cage SystemK202190 · OVD | 510(k) clearances |
| Sep 24, 2020 | Cavetto-SA Cervical Cage SystemK200115 · OVE | 510(k) clearances |
| Sep 3, 2020 | Cavetto [MAX] Cervical Cage SystemK201769 · ODP | 510(k) clearances |
| Jul 24, 2020 | Transept Cervical Plate SystemK200927 · KWQ | 510(k) clearances |
| Nov 25, 2019 | Cortina™ [MAX] Lumbar Cage SystemK192248 · MAX | 510(k) clearances |
| Nov 9, 2018 | Arco™-SA Lumbar Cage SystemK182195 · OVD | 510(k) clearances |
| Nov 8, 2018 | Neurostructures Cavetto® [MAX] Cervical Cage SystemK181590 · ODP | 510(k) clearances |
| Mar 29, 2018 | Arco™-SA Lumbar Cage SystemK173082 · OVD | 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
