510(k) K243973 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FIX-L PEEK PLIF and T-PLIF System
| Applicant | Jeil Medical Corporation, Seoul, KR |
| Decision | Substantially Equivalent, Jun 12, 2025 |
| Received | Dec 23, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243973
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.