510(k) K131671 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MECTALIF
| Applicant | Medacta International, Camarillo CA, US |
| Decision | Substantially Equivalent, Jul 5, 2013 |
| Received | Jun 7, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131671
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.