510(k) K032454 ยท DZE Implant, Endosseous, Root-Form
SILHOUETTE(TM) IC OR SILHOUETTE(TM) & LASER-LOK (TM)
| Applicant | Bio-Lok Intl., Inc., Stillwater MN, US |
| Decision | Substantially Equivalent, Mar 4, 2004 |
| Received | Aug 11, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032454
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.