510(k) K172064 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Ti-Diagon Oblique TLIF
| Applicant | Camber Spine Technologies, Wayne PA, US |
| Decision | Substantially Equivalent, Sep 15, 2017 |
| Received | Jul 7, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172064
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.