Class Class II

Rosa Knee System (K230180)

K230180 2023-02-22 Special
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Description

Rosa Knee System by Orthosoft Inc (D/B/A Zimmer Cas) — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230180
Clearance Date2023-02-22
Clearance TypeSpecial
Product CodeOLO
Regulation Number882.4560

Categories

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