510(k) K020344 ยท JDK Prosthesis, Hip, Cement Restrictor
RPX TITANIUM CEMNT RESTRICTOR
| Applicant | Sulzer Spine-Tech, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 2, 2002 |
| Received | Feb 1, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020344
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.