510(k) K141405 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MOBIS II ST SPINAL IMPLANT
| Applicant | Signus Medizintechnik GmbH, Round Rock TX, US |
| Decision | Substantially Equivalent, Sep 16, 2014 |
| Received | May 28, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141405
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.