Class Class II

EXULT Knee Replacement System (K242046)

K242046 2024-08-01 Special
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Description

EXULT Knee Replacement System by Corentec Co., Ltd. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242046
Clearance Date2024-08-01
Clearance TypeSpecial
Product CodeJWH
Regulation Number888.3560

Categories

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