510(k) K133459 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ELITE IBF
| Applicant | Innova Spinal Technologies, LLC, Fr. Myers FL, US |
| Decision | Unknown, Mar 6, 2014 |
| Received | Nov 12, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133459
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.