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Spineex, Inc.

3 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices (K200816)Spineex, Inc.2020-04-30
SpineEX Sagittae® Lateral Lumbar Interbody Fusion Devices (K190193)Spineex, Inc.2019-03-04
SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices (K181531)Spineex, Inc.2018-10-05

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