510(k) K120293 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DRIVE
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Feb 29, 2012 |
| Received | Jan 31, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120293
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.