510(k) K222988 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical
| Applicant | Ht Medical D.B.A. Xenix Medical, Orlando FL, US |
| Decision | Substantially Equivalent, Sep 1, 2023 |
| Received | Sep 28, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222988
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.