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U.S. Department of Health and Human Services

Medical Device Recalls

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Related Medical Device Recalls
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Z-1912-2018 - AMENDIA Omega Lumbar Interbody Fusion Device, Part Number 72-00-2-092812-11 The OmegaLIF(TM) (LIF(TM)) Expandable Lumbar Interbody Device is designed for use in intervertebral body spinal fusion pr... 2 05/23/2018 Spinal Elements
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