K-number	K041965
Device name	ARTHREX HUMERAL FRACTURE PLATES AND SCREWS
Applicant	Arthrex, Inc.
Product code	HRS
Device class	Class II
Decision date	Sep 8, 2004
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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ARTHREX HUMERAL FRACTURE PLATES AND SCREWS

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