510(k) K011904 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
NEXGEN PRIMARY POROUS PATELLA, MODEL 04-211-IIII-5878-65-ZZ-(STANDARD),04-212-IIII-5878-61-ZZ-(MICRO)
| Applicant | Implex Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Jul 19, 2001 |
| Received | Jun 19, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K011904
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.