510(k) K080673 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Vertebral Technologies, Inc., Andover MN, US |
| Decision | Substantially Equivalent, Jun 10, 2008 |
| Received | Mar 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080673
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.