Class Class II

OsteoSight™ Hip (v1) (K251408)

K251408 2025-09-02 Traditional
Home/ Devices/ OsteoSight™ Hip (v1) (K251408)

Description

OsteoSight™ Hip (v1) by Naitive Technologies, Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251408
Clearance Date2025-09-02
Clearance TypeTraditional
Product CodeSAO
Regulation Number892.1171

Categories

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