510(k) K981858 ยท DZE Implant, Endosseous, Root-Form
ATLANTIS ABUTMENT AND ATLANTIS ABUTMENT SCREW
| Applicant | Atlantis Components, Inc., Cambridge MA, US |
| Decision | Substantially Equivalent, Mar 22, 1999 |
| Received | May 27, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981858
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.