510(k) K123207 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PRIMALIF TM LLIF UNITARY PEEK LATERAL LUMBAR INTERBODY FUSION SYSTEM
| Applicant | Osteomed LP, Addison TX, US |
| Decision | Substantially Equivalent, Nov 29, 2012 |
| Received | Oct 12, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123207
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.