Class Class II

Curiteva Porous PEEK Cervical Interbody Fusion System (K254061)

K254061 2026-01-15 Special
Home/ Devices/ Curiteva Porous PEEK Cervical…

Description

Curiteva Porous PEEK Cervical Interbody Fusion System by Curiteva, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK254061
Clearance Date2026-01-15
Clearance TypeSpecial
Product CodeODP
Regulation Number888.3080

Categories

Need More Information?

Contact the manufacturer or request a quote for this device.

Request Quote
Scroll to Top