510(k) K193521 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Steerable Plateau Ti
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Feb 6, 2020 |
| Received | Dec 19, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193521
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.