510(k) K202034 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
aprevo Intervertebral Body Fusion Device
| Applicant | Carlsmed, Inc., La Jolla CA, US |
| Decision | Substantially Equivalent, Dec 3, 2020 |
| Received | Jul 23, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202034
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.