510(k) K183243 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Velofix TLIF Cage
| Applicant | U&I Corporation, Uijeongbu-Si, KR |
| Decision | Substantially Equivalent, Jul 10, 2019 |
| Received | Nov 21, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K183243
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.