510(k) K232282 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
aprevo® anterior and lateral lumbar interbody fusion device, aprevo® transforaminal lumbar interbody fusion device
| Applicant | Carlsmed, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Mar 22, 2024 |
| Received | Jul 31, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232282
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.