K-number	K081348
Device name	TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD
Applicant	TriMed, Inc.
Product code	MBI
Device class	Class II
Decision date	Oct 17, 2008
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD

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