510(k) K071851 ยท DZE Implant, Endosseous, Root-Form
HDC STERILE SPIDER SCREW
| Applicant | Hdc S.R.L., S. Lazzaro Di Savena, Bologna, IT |
| Decision | Substantially Equivalent, Oct 18, 2007 |
| Received | Jul 5, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071851
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.