510(k) K221324 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)
| Applicant | Camber Spine Technologies, King Of Prussia PA, US |
| Decision | Substantially Equivalent, Mar 30, 2023 |
| Received | May 6, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221324
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.