510(k) K221894 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Lumbar Expandable lnterbody Spacers -Additional Indications/Implants
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Aug 3, 2023 |
| Received | Jun 30, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221894
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.