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 Nexxt Spine with 24 510(k) clearances. The most recent is a 510(k) clearance dated Mar 14, 2025: NEXXT MATRIXX® SI 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 14, 2025 | NEXXT MATRIXX® SI SystemK243838 · OUR | 510(k) clearances |
| Mar 22, 2024 | STRUXXURE® MCS Anterior Cervical Plate SystemK240690 · KWQ | 510(k) clearances |
| Jul 20, 2023 | INERTIA® CONNEXX™ Modular Pedicle Screw SystemK231799 · NKB | 510(k) clearances |
| Jul 28, 2022 | INERTIA CONNEXX Modular Pedicle Screw SystemK221905 · NKB | 510(k) clearances |
| Mar 31, 2022 | NEXXT SPINE NAVIGATION SystemK220291 · OLO | 510(k) clearances |
| Dec 15, 2020 | NEXXT MATRIXX Stand Alone ALIF SystemK202230 · OVD | 510(k) clearances |
| Sep 17, 2020 | STRUXXURE®-L and STRUXXURE®-A Plate SystemK202192 · KWQ | 510(k) clearances |
| May 21, 2020 | NEXXT MATRIXX SystemK200969 · 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
