510(k) K050408 ยท DZE Implant, Endosseous, Root-Form
BICON ORTHODONTIC IMPLANT SYSTEM
| Applicant | Bicon, Inc., Boston MA, US |
| Decision | Substantially Equivalent, Apr 7, 2005 |
| Received | Feb 17, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050408
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.