510(k) K210728 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONDUIT Instruments
| Applicant | Medos International SARL, Lelocle, CH |
| Decision | Substantially Equivalent, May 6, 2021 |
| Received | Mar 11, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210728
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.