510(k) K192115 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SABLE Expandable Spacer
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Jan 14, 2020 |
| Received | Aug 6, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192115
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.