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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
Related Medical Device Recalls
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Z-0393-2019 - Biomet Microfixation RapidFlap System 12mm SpinDown Clamp, sterile Ref Number: 75-1020 Used for the re-attachment of the bone flap after a craniotomy. 2 11/06/2018 FEI # 1825034
Zimmer Biomet, Inc.
Z-0394-2019 - Biomet Microfixation RapidFlap System, 12MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1020-12 Used for the re-attachment of the bone flap after a craniotomy. 2 11/06/2018 FEI # 1825034
Zimmer Biomet, Inc.
Z-0398-2019 - Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1040-12 Used for the re-attachment of the bone flap after a craniotomy. 2 11/06/2018 FEI # 1825034
Zimmer Biomet, Inc.
Z-0396-2019 - Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1030-12 Used for the re-attachment of the bone flap after a craniotomy. 2 11/06/2018 FEI # 1825034
Zimmer Biomet, Inc.
Z-0397-2019 - Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp Ref Number: 75-1040 Used for the re-attachment of the bone flap after a craniotomy. 2 11/06/2018 FEI # 1825034
Zimmer Biomet, Inc.
Z-0395-2019 - Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Ref Number: 75-1030 Used for the re-attachment of the bone flap after a craniotomy. 2 11/06/2018 FEI # 1825034
Zimmer Biomet, Inc.
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