510(k) K162402 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
4CIS® Marlin ACIF Cage System
| Applicant | Solco Biomedical Co., Ltd., Pyeongtaek, KR |
| Decision | Substantially Equivalent, Feb 16, 2017 |
| Received | Aug 26, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162402
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.