Class Class II

SPINEART Navigation Instrument System (K242933)

K242933 2025-06-18 Traditional
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Description

SPINEART Navigation Instrument System by Spineart SA, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242933
Clearance Date2025-06-18
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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