510(k) K012551 ยท KWI Prosthesis, Elbow, Hemi-, Radial, Polymer
LIVERPOOL RADIAL HEAD REPLACEMENT DEVICE
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 30, 2002 |
| Received | Aug 7, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012551
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.