510(k) K172828 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Double Medical Cage System
| Applicant | Double Medical Technology, Inc., Xiamen, CN |
| Decision | Substantially Equivalent, Feb 1, 2018 |
| Received | Sep 18, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172828
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.