510(k) K032108 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
SEARCH EVOLUTION (LC) TOTAL KNEE SYSTEM (POROUS COATED)
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jan 15, 2004 |
| Received | Jul 8, 2003 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K032108
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.