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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.
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.
K223200
10/13/2022
Curiteva Navigation System
Curiteva, Inc.
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