Class Class II

xvision Spine system (K251639)

K251639 2025-10-03 Traditional
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Description

xvision Spine system by Augmedics, Ltd., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251639
Clearance Date2025-10-03
Clearance TypeTraditional
Product CodeSBF
Regulation Number882.4560

Categories

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