510(k) K173537 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONCORDE LIFT
| Applicant | Medos International SARL, Lelocle, CH |
| Decision | Substantially Equivalent, Feb 8, 2018 |
| Received | Nov 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173537
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.