Class Class II

ACTIVBRAID™ (K223822)

K223822 2023-06-02 Traditional
Home/ Devices/ ACTIVBRAID™ (K223822)

Description

ACTIVBRAID™ by Embody, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223822
Clearance Date2023-06-02
Clearance TypeTraditional
Product CodeGAT
Regulation Number878.5000

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