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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K081501
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10mm X 12o Solitaire Ti Medium Spacer  Solitaire Anterior Spinal System, Model Number 1400-1230. ... 2 03/25/2016 FEI # 3012447612
Biomet Spine, LLC
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