510(k) K091988 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076
| Applicant | Vertebral Technologies, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 30, 2009 |
| Received | Jul 2, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K091988
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.