510(k) K113478 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PLIF CAGE
| Applicant | Eisertech, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Mar 5, 2012 |
| Received | Nov 23, 2011 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K113478
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.