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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K981251
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Recall
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Extremities, Large Kit Assy, US, 15/3 - Product Usage: is an injectable, moldable and biocompatible ... 2 06/16/2020 Medtronic Sofamor Danek USA Inc
Medtronic Bone Void Filler, Large - Product Usage: is an injectable, moldable and biocompatible ca... 2 06/16/2020 Medtronic Sofamor Danek USA Inc
Medtronic Bone Void Filler, Small - Product Usage: is an injectable, moldable and biocompatible ca... 2 06/16/2020 Medtronic Sofamor Danek USA Inc
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