510(k) K120203 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TM-400 DEVICE
| Applicant | Zimmer Trabecular Metal Technology, Inc., Parsippany NJ, US |
| Decision | Substantially Equivalent, Jun 15, 2012 |
| Received | Jan 23, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120203
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.