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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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