510(k) K203254 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Lucent 3D Spinal System
| Applicant | Spinal Elements, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Mar 26, 2021 |
| Received | Nov 4, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203254
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.