510(k) K151615 ยท JDR Staple, Fixation, Bone
TiTHON Staple with OsseoTi Technology
| Applicant | Biomet Manufacturing Corp, Warsaw IN, US |
| Decision | Substantially Equivalent, Oct 2, 2015 |
| Received | Jun 15, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151615
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.