510(k) K022425 ยท DZE Implant, Endosseous, Root-Form
SCREWLINE
| Applicant | Altatec Biotechnologies N.A., Inc., Potomac MD, US |
| Decision | Substantially Equivalent, Aug 14, 2002 |
| Received | Jul 24, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022425
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.