510(k) K110067 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
LP CAGE
| Applicant | Medyssey Co, Ltd., Apple Valley MN, US |
| Decision | Substantially Equivalent, Apr 8, 2011 |
| Received | Jan 10, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110067
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.