510(k) K133371 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
RAMPART-L
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Jan 9, 2014 |
| Received | Nov 1, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133371
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.