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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
510(K) Number: K031034
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Product Description
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FDA Recall
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Biomet Microfixation RapidFlap System 12mm SpinDown Clamp, sterile Ref Number: 75-1020 Used for th... 2 11/06/2018 Zimmer Biomet, Inc.
Biomet Microfixation RapidFlap System, 12MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1020-... 2 11/06/2018 Zimmer Biomet, Inc.
Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1040-... 2 11/06/2018 Zimmer Biomet, Inc.
Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-103... 2 11/06/2018 Zimmer Biomet, Inc.
Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Ref Number: 75-1040 Used fo... 2 11/06/2018 Zimmer Biomet, Inc.
Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Ref Number: 75-1030 Used fo... 2 11/06/2018 Zimmer Biomet, Inc.
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