Medical Device Recalls
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61 to 65 of 65 Results
510(K) Number: K951185 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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REF 90-5970-031-10, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... | 2 | 05/14/2012 | Zimmer Inc. |
REF 90-5970-031-12, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... | 2 | 05/14/2012 | Zimmer Inc. |
REF 90-5970-031-14, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... | 2 | 05/14/2012 | Zimmer Inc. |
REF 90-5970-031-17, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... | 2 | 05/14/2012 | Zimmer Inc. |
REF 90-5972-031-20, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... | 2 | 05/14/2012 | Zimmer Inc. |
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