OsteoSight Hip (v1)— 510(k) K251408

Substantially Equivalent

Naitive Technologies, Ltd.

FDA 510(k) clearance K251408 for OsteoSight Hip (v1), Substantially Equivalent on 2025-09-02. Applicant: Naitive Technologies, Ltd.. Device class: 2.

Clearance details

Applicant
Naitive Technologies, Ltd.
Product code
Code SAO
Device class
Class 2
Regulation
21 CFR 892.1171
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Cambridge, GB
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