510(k) K211689 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
KEYSTONE PEEK Cage System
| Applicant | Shanghai Sanyou Medical Co, Ltd., Jiading District, CN |
| Decision | Substantially Equivalent, Sep 21, 2021 |
| Received | Jun 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211689
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.