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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K002335
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Natural-Knee II Durasul All-Poly Patella, Size 0, 7mm The Zimmer Natural-Knee II Durasul Patella ... 2 01/25/2012 Zimmer Inc.
Natural-Knee II Durasul All-Poly Patella, Size 1, 7mm The Zimmer Natural-Knee II Durasul Patella ... 2 01/25/2012 Zimmer Inc.
Natural-Knee II Durasul All-Poly Patella, Size 2, 7mm The Zimmer Natural-Knee II Durasul Patella ... 2 01/25/2012 Zimmer Inc.
Natural-Knee II Durasul All-Poly Patella, Size 3, 10mm The Zimmer Natural-Knee II Durasul Patella... 2 01/25/2012 Zimmer Inc.
Natural-Knee II Durasul All-Poly Patella, Size 0, 10mm The Zimmer Natural-Knee II Durasul Patella... 2 01/25/2012 Zimmer Inc.
Natural-Knee II Durasul All-Poly Patella, Size 1, 10mm The Zimmer Natural-Knee II Durasul Patella... 2 01/25/2012 Zimmer Inc.
Natural-Knee II Durasul All-Poly Patella, Size 2, 10mm The Zimmer Natural-Knee II Durasul Patella... 2 01/25/2012 Zimmer Inc.
Natural-Knee II Durasul All-Poly Patella, Size 3, 7mm The Zimmer Natural-Knee II Durasul Patella ... 2 01/25/2012 Zimmer Inc.
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