510(k) K020345 ยท KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
ARTHREX UNIVERS FRACTURE PROSTHESIS
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Sep 6, 2002 |
| Received | Feb 1, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020345
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.