510(k) K950563 ยท KWL Prosthesis, Hip, Hemi-, Femoral, Metal
ULTIMA AUGMENTED UHMWPE CUP
| Applicant | Johnson & Johnson Professionals, Inc., Raritan NJ, US |
| Decision | Substantially Equivalent, Jun 7, 1995 |
| Received | Feb 8, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950563
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.