510(k) K090899 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DEPUY SPINE LATERAL SYSTEM
| Applicant | Depuy Spine, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, May 19, 2009 |
| Received | Apr 1, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090899
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.