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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K152156
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FDA Recall
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Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (... 2 04/27/2019 DePuy Spine, Inc.
G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180-07, 9180-1... 2 01/03/2017 Interventional Spine Inc
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