510(k) K000100 ยท DZE Implant, Endosseous, Root-Form
CAMLOG ROOTFORM IMPLANT SYSTEM
| Applicant | Altatec Biotechnologies, Potomac MD, US |
| Decision | Substantially Equivalent, Jan 28, 2000 |
| Received | Jan 13, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000100
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.