510(k) K113003 ยท NHA Abutment, Implant, Dental, Endosseous
ATLANTIS(TM) ABUTMENT AND ATLANTIS(TM) CROWN ABUTMENT FOR KEYSTONE GENESIS IMPLANT, ATLANTIS GEMINI(TM) ABUTMENT...
| Applicant | Astra Tech, Inc., Skokie IL, US |
| Decision | Substantially Equivalent, Mar 1, 2012 |
| Received | Oct 7, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113003
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.