510(k) K101301 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
STALIF MIDLINE
| Applicant | Centinel Spine, Washington DC, US |
| Decision | Substantially Equivalent, Sep 24, 2010 |
| Received | May 10, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101301
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.