510(k) K082128 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DEPUY SPINE LATERAL CAGE SYSTEM
| Applicant | Depuy Spine, Raynham MA, US |
| Decision | Substantially Equivalent, Nov 14, 2008 |
| Received | Jul 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082128
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.