510(k) K210542 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
aprevo Transforaminal IBF
| Applicant | Carlsmed, Inc., La Jolla CA, US |
| Decision | Substantially Equivalent, Jun 30, 2021 |
| Received | Feb 24, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210542
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.