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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K133827
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Link Z Ti Unitary Plate-Cage 3... 2 06/11/2020 FEI # 3010866843
Acuity Surgical Devices, LLC
A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Link Z Ti Unitary Open Interbo... 2 06/11/2020 FEI # 3010866843
Acuity Surgical Devices, LLC
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