510(k) K080418 ยท NUN Bone Grafting Material, Human Source
REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST
| Applicant | Regeneration Technologies, Inc., Alachua FL, US |
| Decision | Substantially Equivalent, Apr 30, 2008 |
| Received | Feb 15, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080418
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.