Class Class II

Genostis Osteosynthesis System (K242988)

K242988 2025-06-27 Traditional
Home/ Devices/ Genostis Osteosynthesis System (K242988)

Description

Genostis Osteosynthesis System by Genostis AF, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242988
Clearance Date2025-06-27
Clearance TypeTraditional
Product CodeHRS
Regulation Number888.3030

Categories

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