510(k) K182470 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Plateau Spacer System
| Applicant | Life Spine, Huntley IL, US |
| Decision | Substantially Equivalent, Nov 26, 2018 |
| Received | Sep 10, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182470
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.