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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