510(k) K060500 ยท DZE Implant, Endosseous, Root-Form
SPEEDY ORTHODONTIC SCREW
| Applicant | Dentium Co., Ltd., Dunwoody GA, US |
| Decision | Substantially Equivalent, Jun 16, 2006 |
| Received | Feb 24, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060500
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.