Class Class II

PUREVUE™ FMS (K250795)

K250795 2025-12-05 Traditional
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Description

PUREVUE™ FMS by W.O.M. World of Medicine GmbH, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250795
Clearance Date2025-12-05
Clearance TypeTraditional
Product CodeHRX
Regulation Number888.1100

Categories

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