Class Class II

VyBrate™ VBR System (K253158)

K253158 2026-01-07 Traditional
Home/ Devices/ VyBrate™ VBR System (K253158)

Description

VyBrate™ VBR System by Vy Spine, LLC, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253158
Clearance Date2026-01-07
Clearance TypeTraditional
Product CodeMQP
Regulation Number888.3060

Categories

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