510(k) K993560 ยท DZE Implant, Endosseous, Root-Form
FRIALIT-2 BONE PROFILER
| Applicant | Friadent GmbH, Lake Forest CA, US |
| Decision | Substantially Equivalent, Jan 10, 2000 |
| Received | Oct 21, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993560
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.