Medical Device Recalls
-
61 to 65 of 65 Results
510(K) Number: K951185 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
00-5976-031-17, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... | 2 | 05/14/2012 | Zimmer Inc. |
00-5976-031-20, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... | 2 | 05/14/2012 | Zimmer Inc. |
00-5970-031-23, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... | 2 | 05/14/2012 | Zimmer Inc. |
00-5972-031-23, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... | 2 | 05/14/2012 | Zimmer Inc. |
00-5976-031-23, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... | 2 | 05/14/2012 | Zimmer Inc. |
-