510(k) K072226 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IMPIX SPACER
| Applicant | Medicrea Technologies, Round Rock TX, US |
| Decision | Substantially Equivalent, Dec 10, 2007 |
| Received | Aug 10, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072226
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.