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U.S. Department of Health and Human Services

Medical Device Recalls
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61 to 70 of 83 Results
510(K) Number: K933785
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REF 00-5970-031-10, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... 2 05/14/2012 Zimmer Inc.
REF 00-5970-031-12, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... 2 05/14/2012 Zimmer Inc.
REF 00-5970-031-14, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... 2 05/14/2012 Zimmer Inc.
REF 00-5970-031-17, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... 2 05/14/2012 Zimmer Inc.
REF 00-5970-031-20, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... 2 05/14/2012 Zimmer Inc.
REF 90-5970-031-09, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate R... 2 05/14/2012 Zimmer Inc.
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.
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