Class Class II

Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF System (K252205)

K252205 2026-01-16 Traditional
Home/ Devices/ Curiteva Porous PEEK Cervical…

Description

Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF System by Curiteva, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252205
Clearance Date2026-01-16
Clearance TypeTraditional
Product CodeODP
Regulation Number888.3080

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top