510(k) K130396 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
RAMPART O AND RAMPART P
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Mar 25, 2013 |
| Received | Feb 19, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K130396
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.