510(k) K241019 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
aprevo® TLIF-C Articulating System
| Applicant | Carlsmed, Carlsbad CA, US |
| Decision | Substantially Equivalent, Jul 9, 2024 |
| Received | Apr 15, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241019
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.