510(k) K141443 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INFRONT LUMBAR INTERBODY FUSION SYSTEM
| Applicant | Infront Medical, LLC, Clifton NJ, US |
| Decision | Substantially Equivalent, Aug 28, 2014 |
| Received | Jun 2, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141443
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.