510(k) K071937 ยท KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction
BONALIVE GRANULES AND BONALIVE PLATES
| Applicant | Vivoxid , Ltd., Findley MN, US |
| Decision | Substantially Equivalent, Oct 19, 2007 |
| Received | Jul 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071937
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.