510(k) K153786 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PROW FUSION-V
| Applicant | Nlt Spine, Ltd., Kfar-Saba, IL |
| Decision | Substantially Equivalent, Jul 11, 2016 |
| Received | Dec 31, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153786
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.