510(k) K223654 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Medussa-PL Cage
| Applicant | Medyssey USA, Inc., Buffalo Grove IL, US |
| Decision | Substantially Equivalent, Dec 28, 2022 |
| Received | Dec 6, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K223654
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.