510(k) K172446 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
SPIRA-C Open Matrix Cervical Interbody
| Applicant | Camber Spine Technologies, Wayne PA, US |
| Decision | Substantially Equivalent, Nov 7, 2017 |
| Received | Aug 14, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172446
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.