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Keos

4 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Keos Anterior Cervical Interbody Fusion Device System (K212450)Keos2022-06-06
Keos Lumbar IBFD (K193174)Keos2019-12-16
Keos Lumbar IBFD (K163386)Keos2017-04-10
Keos Lumbar IBFD (K160631)Keos2016-07-15

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Every clearance here is in the API, with alerts when new ones post.