510(k) K170550 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Coveris Cervical Cage System
| Applicant | Camber Spine Technologies, Wayne PA, US |
| Decision | Substantially Equivalent, Jul 13, 2017 |
| Received | Feb 24, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170550
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.