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Keos

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories2
Latest Approval2022-06-06
TypeNumberDevice NameCodeDate
510(k) K212450 Keos Anterior Cervical Interbody Fusion Device System ODP 2022-06-06 View
510(k) K193174 Keos Lumbar IBFD MAX 2019-12-16 View
510(k) K163386 Keos Lumbar IBFD MAX 2017-04-10 View
510(k) K160631 Keos Lumbar IBFD MAX 2016-07-15 View
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