510(k) K112496 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PIONEER CROSSFUSE II IBF/VBR SYSTEM
| Applicant | Pioneer Surgical Technology, Inc., Marquette MI, US |
| Decision | Substantially Equivalent, Sep 28, 2011 |
| Received | Aug 29, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112496
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.