Medical Device Manufacturer · US , Tanner , AL

Curiteva, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2019

Recent clearances: Curiteva Porous PEEK Cervical Interbody System, Curiteva Porous PEEK Cervical Interbody Fusion System, Curiteva Porous PEEK Standalone ALIF System

11
Total
11
Cleared
0
Denied

FDA 510(k) Regulatory Record - Curiteva, Inc. Orthopedic ✕

11 devices
1-11 of 11
Cleared Jan 16, 2026
Curiteva Porous PEEK Cervical Interbody System
K252205 · ODP
Orthopedic · 186d
Cleared Jan 15, 2026
Curiteva Porous PEEK Cervical Interbody Fusion System
K254061 · ODP
Orthopedic · 29d
Cleared Jun 18, 2025
Curiteva Porous PEEK Standalone ALIF System
K250845 · OVD
Orthopedic · 90d
Cleared Oct 28, 2024
Curiteva Porous PEEK Laminoplasty System
K243137 · NQW
Orthopedic · 28d
Cleared Feb 29, 2024
Curiteva Thoracolumbar Plate System
K233360 · KWQ
Orthopedic · 153d
Cleared Jan 18, 2024
Curiteva Porous PEEK Lumbar Interbody Fusion System
K233744 · MAX
Orthopedic · 57d
Cleared Jun 28, 2023
Curiteva Laminoplasty System
K231232 · NQW
Orthopedic · 61d
Cleared Feb 13, 2023
Curiteva Porous PEEK Cervical Interbody Fusion System
K213030 · ODP
Orthopedic · 510d
Cleared Jan 06, 2023
Curiteva Navigation System
K223200 · OLO
Orthopedic · 85d
Cleared Sep 09, 2021
Curiteva Sacroiliac Joint Fusion System
K210402 · OUR
Orthopedic · 211d
Cleared Aug 28, 2019
Curiteva Pedicle Screw System
K191810 · NKB
Orthopedic · 54d
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