510(k) K980801 ยท KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
J-FX BIPOLAR HEAD
| Applicant | Johnson & Johnson Professionals, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, May 29, 1998 |
| Received | Mar 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980801
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.