510(k) K031568 ยท DZE Implant, Endosseous, Root-Form
BICONITE SURFACE TREATMENT
| Applicant | Bicon, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Nov 23, 2004 |
| Received | May 20, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031568
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.