Class Class II

TECHFIT Diagnostic Models (K222577)

K222577 2023-01-06 Traditional
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Description

TECHFIT Diagnostic Models by Techfit Digital Surgery, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222577
Clearance Date2023-01-06
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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