Class Class II

Naviswiss Knee (K223351)

K223351 2023-01-31 Traditional
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Description

Naviswiss Knee by Naviswiss AG — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223351
Clearance Date2023-01-31
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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