510(k) K231140 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
aprevo® transforaminal lumbar interbody fusion device
| Applicant | Carlsmed, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, May 19, 2023 |
| Received | Apr 21, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231140
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.