510(k) K173080 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IVA Cage Ti (ACIF, PLIF, TLIF, DLIF, and ALIF)
| Applicant | Huvexel Co. , Ltd., Seongnam-Si, KR |
| Decision | Substantially Equivalent, Oct 31, 2017 |
| Received | Sep 29, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173080
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.