Class Class II

Genesys Spine AIS-C II Cervical Interbody Fusion System (K242483)

K242483 2025-02-07 Traditional
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Description

Genesys Spine AIS-C II Cervical Interbody Fusion System by Genesys Spine, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242483
Clearance Date2025-02-07
Clearance TypeTraditional
Product CodeOVE
Regulation Number888.3080

Categories

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