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Curiteva, Inc.

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories8
Latest FDA decision2026-01-16
TypeNumberDevice NameCodeDateActions
510(k) K252205 Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF SystemODP2026-01-16 View
510(k) K254061 Curiteva Porous PEEK Cervical Interbody Fusion SystemODP2026-01-15 View
510(k) K250845 Curiteva Porous PEEK Standalone ALIF SystemOVD2025-06-18 View
510(k) K243137 Curiteva Porous PEEK Laminoplasty SystemNQW2024-10-28 View
510(k) K233360 Curiteva Thoracolumbar Plate SystemKWQ2024-02-29 View
510(k) K233744 Curiteva Porous PEEK Lumbar Interbody Fusion SystemMAX2024-01-18 View
510(k) K231232 Curiteva Laminoplasty SystemNQW2023-06-28 View
510(k) K213030 Curiteva Porous PEEK Cervical Interbody Fusion SystemODP2023-02-13 View
510(k) K223200 Curiteva Navigation SystemOLO2023-01-06 View
510(k) K210402 Curiteva Sacroiliac Joint Fusion SystemOUR2021-09-09 View
510(k) K191810 Curiteva Pedicle Screw SystemNKB2019-08-28 View
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