510(k) K133340 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SPINEWORKS ANTERIOR LUMBAR DEVICE
| Applicant | Spineworks, LLC, Vero Beach FL, US |
| Decision | Substantially Equivalent, Apr 11, 2014 |
| Received | Oct 30, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133340
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.