510(k) K211740 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DualX
| Applicant | Amplify Surgical, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 29, 2021 |
| Received | Jun 7, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K211740
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.