Class Class II

Rosa® Knee System (K251314)

K251314 2025-11-13 Traditional
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Description

Rosa® Knee System by Orthosoft Inc. (d/b/a) Zimmer CAS, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251314
Clearance Date2025-11-13
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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