510(k) K131216 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
RAMPART O
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, May 30, 2013 |
| Received | Apr 30, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131216
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.