Class Class II

Spine & Trauma Navigation Instruments (K252562)

K252562 2025-09-12 Special
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Description

Spine & Trauma Navigation Instruments by Brainlab AG, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252562
Clearance Date2025-09-12
Clearance TypeSpecial
Product CodeOLO
Regulation Number882.4560

Categories

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