510(k) K190483 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SPIRA Open Matrix ALIF and LLIF
| Applicant | Camber Spine Technologies, King Of Prussia PA, US |
| Decision | Substantially Equivalent, Sep 23, 2019 |
| Received | Feb 27, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190483
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.