510(k) K972313 ยท DZE Implant, Endosseous, Root-Form
THE MAESTRO SYSTEM
| Applicant | BioHorizons Implant Systems, Inc., Birmingham AL, US |
| Decision | Substantially Equivalent, Sep 16, 1997 |
| Received | Jun 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972313
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.