Class Class II

KLS Martin Pure Pectus System (K250988)

K250988 2025-12-11 Traditional
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Description

KLS Martin Pure Pectus System by KLS-Martin L.P., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250988
Clearance Date2025-12-11
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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