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 14, 2026, FDA's public records list Altus Partners with 18 510(k) clearances. The most recent is a 510(k) clearance dated May 8, 2025: Altus Spine Navigation 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.
| May 8, 2025 | Altus Spine Navigation SystemK243419 · OLO | 510(k) clearances |
| Sep 16, 2022 | Altus Spine Pedicle Screw SystemK211027 · NKB | 510(k) clearances |
| Apr 19, 2022 | Altus Spine Interbody Standalone Fusion SystemK211837 · OVD | 510(k) clearances |
| Aug 20, 2021 | Altus Spine Sochi OCT Spinal SystemK210887 · NKG | 510(k) clearances |
| Jan 26, 2021 | Altus Spine HA Pedicle Screw SystemK200922 · NKB | 510(k) clearances |
| Jun 2, 2020 | Altus Spine Pedicle Screw SystemK200322 · NKB | 510(k) clearances |
| May 29, 2019 | Fuji Cervical Plate SystemK183084 · KWQ | 510(k) clearances |
| Feb 22, 2019 | Altus Spine Interbody Fusion SystemK182406 · MAX | 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
