510(k) K221325 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONDUIT Lateral Switch Plate
| Applicant | Medos International SARL, Lelocle, CH |
| Decision | Substantially Equivalent, Aug 25, 2022 |
| Received | May 6, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221325
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.