510(k) K110045 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE
| Applicant | Vertebral Technologies, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 3, 2011 |
| Received | Jan 6, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110045
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.