Curiteva, Inc.
Curiteva, Inc. holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2026.
Top product codes for Curiteva, Inc.
Recent clearances by Curiteva, Inc.
- K252205 — Curiteva Porous PEEK Cervical Interbody System +3 more
- K254061 — Curiteva Porous PEEK Cervical Interbody Fusion System
- K250845 — Curiteva Porous PEEK Standalone ALIF System
- K243137 — Curiteva Porous PEEK Laminoplasty System
- K233360 — Curiteva Thoracolumbar Plate System
- K233744 — Curiteva Porous PEEK Lumbar Interbody Fusion System
- K231232 — Curiteva Laminoplasty System
- K213030 — Curiteva Porous PEEK Cervical Interbody Fusion System
- K223200 — Curiteva Navigation System
- K210402 — Curiteva Sacroiliac Joint Fusion System
- K191810 — Curiteva Pedicle Screw System
Data sourced from openFDA. This site is unofficial and independent of the FDA.