FDA 510(k) Applications Submitted by Curiteva, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K181261 05/11/2018 Curiteva Cervical Interbody Fusion System Curiteva, LLC
K181549 06/12/2018 Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System) Curiteva, LLC
K181562 06/14/2018 Curiteva Anterior Cervical Plate System Curiteva, LLC
K181589 06/18/2018 Curiteva Lumbar Interbody Fusion System Curiteva, LLC


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