510(k) K230942 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SPIRA® Posterior Lumbar Spacers
| Applicant | Camber Spine Technologies, King Of Prussia PA, US |
| Decision | Substantially Equivalent, Jul 11, 2023 |
| Received | Apr 3, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230942
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.