510(k) K021822 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
R120 MODULAR TOTAL HIP SYSTEM
| Applicant | Osteoimplant Technology, Inc., Hunt Valley MD, US |
| Decision | Substantially Equivalent, Jul 23, 2002 |
| Received | Jun 4, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021822
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.