510(k) K102277 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
| Applicant | Vertebral Technologies, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 6, 2010 |
| Received | Aug 11, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K102277
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.