510(k) K241328 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
aprevo® Anterior and Lateral Lumbar Interbody Fusion device (ALIF/LLIF); aprevo® Transforaminal Lumbar Interbody Fusion device (TLIF); aprevo® Anterior Lumbar Interbody Fusion device with Interfixation (ALIF-X)
| Applicant | Carlsmed, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Aug 12, 2024 |
| Received | May 10, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241328
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.