Class Class II

Pectus Versa System (K251050)

K251050 2025-12-19 Traditional
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Description

Pectus Versa System by Gm Dos Reis Industria E Comercio, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251050
Clearance Date2025-12-19
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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