Class Class II

PathKeeper System (K222355)

K222355 2023-03-08 Traditional
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Description

PathKeeper System by Pathkeeper Surgical , Ltd. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222355
Clearance Date2023-03-08
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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