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Curiteva, LLC

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

Total Devices4
Categories3
Latest FDA decision2018-12-20
TypeNumberDevice NameCodeDateActions
510(k) K181589 Curiteva Lumbar Interbody Fusion SystemMAX2018-12-20 View
510(k) K181549 Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System)KWQ2018-08-03 View
510(k) K181562 Curiteva Anterior Cervical Plate SystemKWQ2018-08-02 View
510(k) K181261 Curiteva Cervical Interbody Fusion SystemODP2018-07-09 View
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