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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: K083388
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Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/L and Synthes TI Matrix Pre-Bent M... 2 07/28/2015 Synthes (USA) Products LLC
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