510(k) K112359 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PROW FUSION
| Applicant | Nlt Spine, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Nov 8, 2011 |
| Received | Aug 16, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112359
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.