Class Class II

Regeneten Bioinductive Implant (K222501)

K222501 2023-05-11 Traditional
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Description

Regeneten Bioinductive Implant by Smith and Nephew, Inc. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222501
Clearance Date2023-05-11
Clearance TypeTraditional
Product CodeOWY
Regulation Number878.3300

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