510(k) K171749 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Velofix(tm) Interbody Fusion System
| Applicant | U&I Corporation, Uijeongbu-Si, Gyeonggi-Do, KR |
| Decision | Substantially Equivalent, Jul 13, 2017 |
| Received | Jun 13, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171749
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.