Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K031034 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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