510(k) K052471 ยท DZE Implant, Endosseous, Root-Form
HDC SPIDER SCREW
| Applicant | Hdc S.R.L., Bethesda MD, US |
| Decision | Substantially Equivalent, Dec 23, 2005 |
| Received | Sep 8, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052471
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.