510(k) K042339 ยท DZE Implant, Endosseous, Root-Form
NEOPLANT IMPLANT SYSTEM
| Applicant | Neobiotech Co., Ltd., Santa Fe Springs CA, US |
| Decision | Substantially Equivalent, Nov 2, 2004 |
| Received | Aug 30, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042339
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.