510(k) K101433 ยท OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
DEPUY ATTUNE KNEE SYSTEM
| Applicant | DePuy Orthopaedics, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Dec 10, 2010 |
| Received | May 21, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101433
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.