510(k) K092162 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
4CIS PEEK, PLIF AND TLIF CAGE SYSTEM
| Applicant | Solco Biomedical Co., Ltd., Rockville MD, US |
| Decision | Substantially Equivalent, Jan 6, 2010 |
| Received | Jul 16, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092162
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.