510(k) K990304 ยท DZE Implant, Endosseous, Root-Form
MODIFICATION TO ASTRA TECH IMPLANT - DENTAL SYSTEM
| Applicant | Astra Tech, Inc., Lexington MA, US |
| Decision | Substantially Equivalent, Jul 15, 1999 |
| Received | Feb 1, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990304
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.