K-number	K052810
Device name	SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM
Applicant	Scandius Biomedical, Inc.
Product code	MBI
Device class	Class II
Decision date	Dec 20, 2005
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM

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