510(k) K203278 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INDEPENDENCE Spacers, HEDRON IA, MAGNIFY-S Spacers, MONUMENT Spacers, InterContinental Plate-Spacer, ELSA Spacers
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Feb 2, 2021 |
| Received | Nov 6, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203278
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.