510(k) K101281 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
VEGA KNEE SYSTEM
| Applicant | Aesculap Implant System, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jul 30, 2010 |
| Received | May 6, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101281
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.