510(k) K241738 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
PYXIS 3D Titanium Cervical Cage system
| Applicant | GS Medical Co., Ltd., Cheongju-Si, KR |
| Decision | Substantially Equivalent, Aug 20, 2024 |
| Received | Jun 17, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241738
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.