510(k) K111792 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MOBIS, MOVAL, SEMIAL, TETRISMODEL PEEK AND TITANIUM, KIMBA MODEL STANDARD AND MINI
| Applicant | Signus Medizintechnik GmbH, Chesterland OH, US |
| Decision | Substantially Equivalent, Mar 5, 2012 |
| Received | Jun 27, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111792
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.