510(k) K213951 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FORZA XP Expandable Spacer System
| Applicant | Orthofix US, LLC, Lewisville TX, US |
| Decision | Substantially Equivalent, Jan 5, 2022 |
| Received | Dec 17, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213951
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.