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510(k) Data Aggregation

K Number

Device Name

MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA

Manufacturer

Date Cleared

2000-08-24

(24 days)

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Regulation Number

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Panel

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N/A

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Device Name :

MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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