510(k) K053384 ยท DZE Implant, Endosseous, Root-Form
FIXATURE MICROTHREAD OSSEOSPEED, A COMPONENT OF THE ASTRA TECH IMPLANT SYSTEM
| Applicant | Astra Tech, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 24, 2006 |
| Received | Dec 5, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053384
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.