510(k) K223837 · OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
SPIRA®-C Integrated Fixation System
| Applicant | Camber Spine Technologies, King Of Prussia PA, US |
| Decision | Substantially Equivalent, Mar 22, 2023 |
| Received | Dec 22, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223837
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.