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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K072619
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NEXGEN GSF POROUS FEMORAL LPS FLEX SIZE F, RIGHT® " These devices are indicated for patients with... 2 03/14/2018 FEI # 1000220733
Zimmer Biomet, Inc.
CR Flex GSF Porous Femoral LPS Flex GSF Porous Femoral LPS Flex Porous Femoral prosthesis, knee, ... 2 02/22/2016 FEI # 1000220733
Zimmer Biomet, Inc.
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