510(k) K181591 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Fixated Asfora BULLET CAGE® (FABC)
| Applicant | Medical Designs, LLC, Sioux Falls SD, US |
| Decision | Substantially Equivalent, Sep 26, 2018 |
| Received | Jun 18, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181591
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.