510(k) K903630 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
PRECISION OSTEOFLEX FEMORAL COMPONENT
| Applicant | Howmedica Corp., Rutherford NJ, US |
| Decision | Substantially Equivalent, Feb 23, 1994 |
| Received | Aug 10, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903630
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.