510(k) K172419 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Velofix TLIF Cage
| Applicant | U&I Corporation, Uijeongbu-Si, KR |
| Decision | Substantially Equivalent, Dec 4, 2017 |
| Received | Aug 10, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172419
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.