510(k) K140577 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INNESIS PEEK TL CAGE
| Applicant | Bk Meditech, Co., Ltd., Stillwater MN, US |
| Decision | Substantially Equivalent, Oct 1, 2014 |
| Received | Mar 6, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140577
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.