510(k) K120024 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MECTALIF TRANSFORAMINAL
| Applicant | Medacta International S.A., Camarillo CA, US |
| Decision | Substantially Equivalent, Feb 28, 2012 |
| Received | Jan 3, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120024
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.