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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K192221
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Product Description
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Recall
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FDA Recall
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ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform, 2 11/03/2021 FEI # 3001617766
Implant Direct Sybron Manufacturing LLC
ImplantDirect, REF 834713, Legacy 2 Implant 4.7mmD x 13mmL, 4.5mmD Platform, 2 11/03/2021 FEI # 3001617766
Implant Direct Sybron Manufacturing LLC
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