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Spineex, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories1
Latest Approval2020-04-30
TypeNumberDevice NameCodeDate
510(k) K200816 SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices MAX 2020-04-30 View
510(k) K190193 SpineEX Sagittae® Lateral Lumbar Interbody Fusion Devices MAX 2019-03-04 View
510(k) K181531 SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices MAX 2018-10-05 View
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