510(k) K230872 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Halis Lumbar Cage System, Lydia Anterior Lumbar Fusion System, Dica Direction Changeable Lumbar Cage System, KEYSTONE Cage System
| Applicant | Shanghai Sanyou Medical Co, Ltd., Jiading District, CN |
| Decision | Substantially Equivalent, Dec 12, 2023 |
| Received | Mar 30, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230872
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.