K-number	K930152
Device name	ARTHREX TIBIAL TUNNEL CANNULA
Applicant	Arthrex, Inc.
Product code	HRX
Device class	Class II
Decision date	Mar 11, 1994
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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ARTHREX TIBIAL TUNNEL CANNULA

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