510(k) K193457 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AUDERE Lumbar Spacer System
| Applicant | Met One Technologies, El Paso TX, US |
| Decision | Substantially Equivalent, May 12, 2020 |
| Received | Dec 16, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193457
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.