510(k) K131071 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
STAXX IBL SYSTEM
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Aug 20, 2013 |
| Received | Apr 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131071
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.