510(k) K142392 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Zavation Posterior LEIF
| Applicant | Zavation, LLC, Flowood MS, US |
| Decision | Substantially Equivalent, Apr 29, 2015 |
| Received | Aug 27, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142392
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.