Class Class II

ClariVy™ Cervical IBF System (K230414)

K230414 2023-05-12 Special
Home/ Devices/ ClariVy™ Cervical IBF System…

Description

ClariVy™ Cervical IBF System by Vy Spine, LLC — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230414
Clearance Date2023-05-12
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