510(k) K180347 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
3d Cage
| Applicant | Fims Co., Ltd., Suwon-Si, KR |
| Decision | Substantially Equivalent, Oct 28, 2019 |
| Received | Feb 8, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180347
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.