510(k) K250987 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
aprevo® posterior/transforaminal lumbar interbody fusion device
| Applicant | Carlsmed, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Jun 30, 2025 |
| Received | Mar 31, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250987
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.