510(k) K223868 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PYXIS 3D Titanium Cage System
| Applicant | GS Medical Co., Ltd., Cheongju-Si, KR |
| Decision | Substantially Equivalent, Apr 26, 2023 |
| Received | Dec 23, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223868
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.