Class Class II

Ortho Device, ADAPTIX 3D Orthopedic Imaging System (K221949)

K221949 2023-01-26 Traditional
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Description

Ortho Device, ADAPTIX 3D Orthopedic Imaging System by Pausch Medical GmbH — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221949
Clearance Date2023-01-26
Clearance TypeTraditional
Product CodeIZF
Regulation Number892.1740

Categories

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