K-number	K052918
Device name	REPROCESSED EXTERNAL FIXATION DEVICES
Applicant	Alliance Medical Corp.
Product code	KTT
Device class	Class II
Decision date	Jan 27, 2006
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 DEVICES

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