FDA 510(k) Applications Submitted by Curiteva, Inc.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K210402	02/10/2021	Curiteva Sacroiliac Joint Fusion System	Curiteva, Inc.
K250845	03/20/2025	Curiteva Porous PEEK Standalone ALIF System	Curiteva, Inc.
K231232	04/28/2023	Curiteva Laminoplasty System	Curiteva, Inc.
K191810	07/05/2019	Curiteva Pedicle Screw System	Curiteva, Inc.
K213030	09/21/2021	Curiteva Porous PEEK Cervical Interbody Fusion System	Curiteva, Inc.
K233360	09/29/2023	Curiteva Thoracolumbar Plate System	Curiteva, Inc.
K243137	09/30/2024	Curiteva Porous PEEK Laminoplasty System	Curiteva, Inc.
K223200	10/13/2022	Curiteva Navigation System	Curiteva, Inc.
K233744	11/22/2023	Curiteva Porous PEEK Lumbar Interbody Fusion System	Curiteva, Inc.