510(k) K131372 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MOBIS II
| Applicant | Signus Medizintechnik GmbH, Chesterland OH, US |
| Decision | Substantially Equivalent, Jul 2, 2013 |
| Received | May 13, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131372
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.