Class Class II

SIros-X System (K252322)

K252322 2025-10-22 Traditional
Home/ Devices/ SIros-X System (K252322)

Description

SIros-X System by Genesys Spine, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252322
Clearance Date2025-10-22
Clearance TypeTraditional
Product CodeOUR
Regulation Number888.3040

Categories

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