510(k) K895639 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
MG II POROUS TOTAL KNEE SYSTEM/METAL-BACK PATELLAR
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent for Some Indications, Feb 8, 1990 |
| Received | Sep 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895639
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.