510(k) K140709 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SKYHAWK INTERBODY FUSION SYSTEM
| Applicant | Orthofix, Inc., Lewisville TX, US |
| Decision | Substantially Equivalent, May 27, 2014 |
| Received | Mar 21, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140709
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.