510(k) K180724 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SPIRA Open Matrix LLIF
| Applicant | Camber Spine Technologies, LLC, Wayne PA, US |
| Decision | Substantially Equivalent, Jun 25, 2018 |
| Received | Mar 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180724
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.