510(k) K101732 ยท DZE Implant, Endosseous, Root-Form
ASTRA TECH IMPLANT SYSTEM
| Applicant | Astra Tech AB, San Diego CA, US |
| Decision | Substantially Equivalent, Feb 23, 2011 |
| Received | Jun 21, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101732
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.