510(k) K223474 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PathLoc-TA Expandable Lumbar Cage System
| Applicant | L&K BIOMED Co., Ltd., Yongin-Si, KR |
| Decision | Substantially Equivalent, Jan 13, 2023 |
| Received | Nov 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223474
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.