510(k) K010528 ยท JDK Prosthesis, Hip, Cement Restrictor
TITANIUM CEMENT RESTRICTOR MATERIAL PEEK
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Unknown, Oct 10, 2001 |
| Received | Feb 23, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010528
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.