510(k) K132907 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PLIF LITE AND TLIF LITE
| Applicant | Sintea Plustek, Fr. Myers FL, US |
| Decision | Substantially Equivalent, Jul 24, 2014 |
| Received | Sep 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132907
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.