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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1350-2018
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Spinal Jaxx Interbody Fusion Device, Model: 100001-511, Size: 9 H x 10 W x 25 L Product Usage: T... 2 04/10/2018 FEI # 3013378904
Neuropro Spinal Jaxx
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