510(k) K032507 ยท KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
INTERLOK BIO-MODULAR HUMERAL STEMS
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Sep 5, 2003 |
| Received | Aug 14, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032507
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.