510(k) K201939 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
GAIA Lumbar Interbody Fusion Device (LIFD) Family
| Applicant | Printerprezz, Fremont CA, US |
| Decision | Substantially Equivalent, Oct 8, 2020 |
| Received | Jul 13, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201939
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.