K-number	K080111
Device name	ARTHREX COMPRESSION STAPLE
Applicant	Arthrex, Inc.
Product code	JDR
Device class	Class II
Decision date	Feb 13, 2008
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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ARTHREX COMPRESSION STAPLE

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