Class Class II

Fraxel® FTX Laser System (K242142)

K242142 2024-08-21 Traditional
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Description

Fraxel® FTX Laser System by Solta Medical — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242142
Clearance Date2024-08-21
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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