510(k) K072363 ยท DZE Implant, Endosseous, Root-Form
NANOTITE PREVAIL,CERTAIN,PARELLEL WALLED,TAPERED,EXTERNAL HEX
| Applicant | Biomet 3i, Inc., Palm Beach Gardens FL, US |
| Decision | Substantially Equivalent, Jan 31, 2008 |
| Received | Aug 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072363
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.