510(k) K994326 ยท KWH Prosthesis, Toe, Constrained, Polymer
ASCENT KNEE SYSTEM
| Applicant | Biomet Manufacturing, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 7, 2000 |
| Received | Dec 22, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K994326
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.