510(k) K131082 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INTERFORM INTERBODY CAGE SYSTEM
| Applicant | Next Orthosurgical, Round Rock TX, US |
| Decision | Substantially Equivalent, Aug 26, 2013 |
| Received | Apr 18, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131082
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.