K-number	K031590
Device name	SECTRA ORTHOPEDIC PACKAGE
Applicant	Sectra-Imtec AB
Product code	LLZ
Device class	Class II
Decision date	Oct 2, 2003
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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SECTRA ORTHOPEDIC PACKAGE

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