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510(k) Data Aggregation

K Number

Device Name

ARTHREX UNIVERS II CA HEADS

Manufacturer

Date Cleared

2013-10-30

(231 days)

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Regulation Number

Type

Panel

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Device Name :

ARTHREX UNIVERS II CA HEADS

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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