510(k) K081666 ยท NHA Abutment, Implant, Dental, Endosseous
ATLANTIS, ATLANTIS GEMINI, ATLANTIS GEMINI+ ABUTMENTS FOR ASTRA OSSEOSPEED 3.0 IMPLANTS
| Applicant | Astra Tech, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Oct 7, 2008 |
| Received | Jun 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081666
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.