510(k) K252351 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
UniSpace® TPLIF Cage
| Applicant | Cg Medtech Co., Ltd., Uijeongbu-Si, KR |
| Decision | Substantially Equivalent, Oct 28, 2025 |
| Received | Jul 29, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K252351
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.