510(k) K251741 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PathLoc Lumbar Interbody Fusion Cage System
| Applicant | L&K BIOMED Co., Ltd., Yongin-Si, KR |
| Decision | Substantially Equivalent, Jul 8, 2025 |
| Received | Jun 6, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K251741
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.