510(k) K223688 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONDUIT Lateral Lumbar Intervertebral Fusion Cage, CONDUIT Instruments
| Applicant | Medos International Sàrl, Le Locle, CH |
| Decision | Substantially Equivalent, Mar 8, 2023 |
| Received | Dec 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223688
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.