510(k) K222009 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
aprevo® anterior lumbar interbody fusion device with interfixation
| Applicant | Carlsmed, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Nov 22, 2022 |
| Received | Jul 7, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222009
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.