510(k) K120464 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INNESIS PEEK CAGE
| Applicant | Bk Meditech, Co., Ltd., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Jan 18, 2013 |
| Received | Feb 15, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120464
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.