K-number	K060522
Device name	SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM
Applicant	Scandius Biomedical, Inc.
Product code	MAI
Device class	Class II
Decision date	Apr 11, 2006
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM

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