510(k) K234150 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Lucent® XP
| Applicant | Spinal Elements, Carlsbad CA, US |
| Decision | Substantially Equivalent, Mar 27, 2024 |
| Received | Dec 29, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234150
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.