510(k) K151785 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Px HA PEEK IBF System
| Applicant | Innovasis, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 14, 2015 |
| Received | Jul 1, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151785
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.