510(k) K083626 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DISTRACTABLE WAVE CAGE
| Applicant | Advanced Medical Technology, Inc., Round Rock TX, US |
| Decision | Substantially Equivalent, Oct 19, 2009 |
| Received | Dec 8, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K083626
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.