510(k) K123652 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Mar 22, 2013 |
| Received | Nov 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123652
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.