510(k) K133126 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
K7 LUMBAR SPACERS
| Applicant | K7, LLC, Chesterland OH, US |
| Decision | Substantially Equivalent, Dec 9, 2013 |
| Received | Sep 30, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133126
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.