510(k) K203014 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
EndoLIF Delta-Cage and DoubleWedge-Cage
| Applicant | Joimax GmbH, Raumfabrik 61, DE |
| Decision | Substantially Equivalent, Sep 1, 2021 |
| Received | Oct 1, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203014
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.