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 13, 2026, FDA's public records list Novastep with 9 510(k) clearances. The most recent is a 510(k) clearance dated Mar 25, 2026: Airlock® Ankle Plating 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 25, 2026 | Airlock® Ankle Plating SystemK260274 · HRS | 510(k) clearances |
| Dec 4, 2023 | arcad® 2.0 Duo & Quadro osteosynthesis compressive staplesK230724 · JDR | 510(k) clearances |
| Aug 30, 2023 | Nexis® compressive screwsK223468 · HWC | 510(k) clearances |
| Dec 14, 2019 | Airlock Centrolock Osteosynthesis Implant SystemK192356 · HRS | 510(k) clearances |
| Aug 13, 2015 | Airlock® osteosynthesis plate systemK151277 · HRS | 510(k) clearances |
| Apr 6, 2015 | Airlock osteosynthesis plate systemK143523 · HRS | 510(k) clearances |
| Feb 19, 2015 | LYNC intramedullary implantK143049 · HTY | 510(k) clearances |
| Feb 6, 2015 | Nexis osteosynthesis compressive screwsK143229 · HWC | 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
