510(k) K210595 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SPIRA-T Oblique Posterior Lumbar Spacers, SPIRA-P Posterior Lumbar Spacers
| Applicant | Camber Spine Technologies, LLC, King Of Prussia PA, US |
| Decision | Substantially Equivalent, Jun 15, 2021 |
| Received | Mar 1, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210595
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.