510(k) K201793 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
EDEN Peek Cage
| Applicant | Jmt Co., Ltd., Yangju-Si, KR |
| Decision | Substantially Equivalent, Sep 13, 2021 |
| Received | Jun 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201793
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.