510(k) K163422 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Shanghai Sanyou PEEK Cage System
| Applicant | Shanghai Sanyou Medical Co, Ltd., Jiading District, CN |
| Decision | Substantially Equivalent, Sep 18, 2017 |
| Received | Dec 6, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163422
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.