510(k) K160699 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
VIRTU Lumbar Spacer System
| Applicant | Met 1 Technologies, LLC, El Paso TX, US |
| Decision | Substantially Equivalent, Aug 1, 2016 |
| Received | Mar 14, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160699
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.