510(k) K133813 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FLXFIT INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Expanding Orthopedics, Inc., Colorado Springs CO, US |
| Decision | Substantially Equivalent, Jul 15, 2014 |
| Received | Dec 16, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133813
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.