510(k) K192434 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DualX Lumbar Intervertebral Body Fusion Device
| Applicant | Amplify Surgical, Inc., Laguna Hills CA, US |
| Decision | Substantially Equivalent, Oct 15, 2019 |
| Received | Sep 5, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192434
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.