510(k) K120966 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DEPUY PULSE LUMBAR CAGE SYSTEM
| Applicant | Medos International SARL, Raynham MA, US |
| Decision | Substantially Equivalent, Jul 3, 2012 |
| Received | Mar 30, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120966
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.