510(k) K911572 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
MG II POROUS COBAL T-CHROME FEMORAL COMPONENT
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 1, 1991 |
| Received | Apr 8, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911572
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 29, 2017 | Zimmer Biomet, Inc. CR PRECOAT FEM COMP SIZE BMR
CR PRECOAT FEM COMP SIZE C/R
CR PRECOAT FEM COMP SIZE D/R
CR PRECOAT FEM COMP SIZE E/R
CR PRECOAT FEM COMP SIZE F/R
CR PRECOAT FEM COMP SIZE G/L
CR PRECOAT FEM COMP SIZE H Terminated |
JWH | None listed |
| Nov 29, 2017 | Zimmer Biomet, Inc. CR OPTION FEM COMP SIZE C/L
CR OPTION FEM COMP SIZE C/R
CR OPTION FEM COMP SIZE D/L
CR OPTION FEM COMP SIZE D/R
CR OPTION FEM COMP SIZE E/L
CR OPTION FEM COMP SIZE E/R
CR OPTION FEM COMP SIZE F/L
CR O Terminated |
JWH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.