FDA 510(k) Applications Submitted by Eric Linder

FDA 510(k) Number	Submission Date	Device Name	Applicant
K210402	02/10/2021	Curiteva Sacroiliac Joint Fusion System	Curiteva, Inc.
K231232	04/28/2023	Curiteva Laminoplasty System	Curiteva, Inc.
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
K191810	07/05/2019	Curiteva Pedicle Screw System	Curiteva, Inc.
K213030	09/21/2021	Curiteva Porous PEEK Cervical Interbody Fusion System	Curiteva, Inc.
K223200	10/13/2022	Curiteva Navigation System	Curiteva, Inc.