510(k) K181829 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Velofix TLIF Cage
| Applicant | U&I Corporation, Uijeongbu-Si, KR |
| Decision | Substantially Equivalent, Nov 14, 2018 |
| Received | Jul 9, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K181829
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.