510(k) K181380 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LnK Lumbar Interbody Fusion Cage System
| Applicant | L&K BIOMED Co., Ltd., Yongin-Si, KR |
| Decision | Substantially Equivalent, Sep 11, 2018 |
| Received | May 24, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181380
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.