K-number	K081342
Device name	REPROCESSED EXTERNAL FIXATION ACCESSORIES
Applicant	Sterilmed, Inc.
Product code	KTT
Device class	Class II
Decision date	Aug 13, 2008
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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REPROCESSED EXTERNAL FIXATION ACCESSORIES

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