510(k) K111512 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
BONEBAC T-PLIF INTERVERTEBRAL BODY FUSION DEVICE SYSTEM
| Applicant | Thompson Mis, Inc., Salem NH, US |
| Decision | Substantially Equivalent, Oct 26, 2011 |
| Received | Jun 1, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111512
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.