Class Class II

OR3O Dual Mobility System (K242375)

K242375 2024-10-07 Traditional
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Description

OR3O Dual Mobility System by Smith & Nephew, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242375
Clearance Date2024-10-07
Clearance TypeTraditional
Product CodeLPH
Regulation Number888.3358

Categories

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