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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
Recall Date to: 11/25/2015 510(K) Number: K031511
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Product Description
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FDA Recall
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Dynesys® Set screw M6 2 11/06/2012 Zimmer, Inc.
Dynesys® Revision + set screw 2 11/06/2012 Zimmer, Inc.
Dynesys® L.I.S. Stabilizing cord Rx, Sterile 2 11/06/2012 Zimmer, Inc.
Dynesys® Universal spacer 6-45 2 11/06/2012 Zimmer, Inc.
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