510(k) K113781 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PANTHEON SPINAL IBFD SYSTEM
| Applicant | Pantheon Spinal, Austin TX, US |
| Decision | Substantially Equivalent, Apr 26, 2013 |
| Received | Dec 22, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113781
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.