510(k) K092193 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SPINAL USA INTERBODY CAGES
| Applicant | Spinal USA, Pear MS, US |
| Decision | Substantially Equivalent, Sep 25, 2009 |
| Received | Jul 21, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092193
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.