510(k) K090425 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
GUIDED LATERAL INTERBODY FUSION (GLIF) SYSTEM
| Applicant | Alphatec Spine, Inc., Carlsnad CA, US |
| Decision | Substantially Equivalent, May 19, 2009 |
| Received | Feb 19, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090425
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.