Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Next Orthosurgical with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 19, 2024: HAnano InterFuse(R) Modular Interbody.
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.
| Sep 19, 2024 | HAnano InterFuse(R) Modular InterbodyK242509 · MAX | 510(k) clearances |
| Jan 15, 2020 | NEX-D2 Posterior Fixation SystemK190981 · NKB | 510(k) clearances |
| Sep 30, 2016 | InterForm Cervical Interbody Cage SystemK161608 · ODP | 510(k) clearances |
| Jul 29, 2016 | VertiForm Posterior Fixation SystemK161499 · NKB | 510(k) clearances |
| Aug 26, 2014 | VERTIFORM POSTERIOR FIXATION SYSTEMK141291 · NKB | 510(k) clearances |
| Aug 26, 2013 | INTERFORM INTERBODY CAGE SYSTEMK131082 · 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
