Class Class II

ACS® LD FB Knee System (K234044)

K234044 2024-09-06 Traditional
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Description

ACS® LD FB Knee System by Implantcast GmbH — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK234044
Clearance Date2024-09-06
Clearance TypeTraditional
Product CodeJWH
Regulation Number888.3560

Categories

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