510(k) K193153 ยท 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, Apr 24, 2020 |
| Received | Nov 13, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193153
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.