510(k) K894331 ยท DZE Implant, Endosseous, Root-Form
OSSEODENT SURGICAL KIT
| Applicant | Collagen Corp., Palo Alto CA, US |
| Decision | Substantially Equivalent, Oct 4, 1989 |
| Received | Jul 14, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894331
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.