Class Class II

Knee+ (K230789)

K230789 2023-04-21 Special
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Description

Knee+ by Pixee Medical — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230789
Clearance Date2023-04-21
Clearance TypeSpecial
Product CodeOLO
Regulation Number882.4560

Categories

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