K-number	K051554
Device name	ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES
Applicant	Alliance Medical Corp.
Product code	KTT
Device class	Class II
Decision date	Jun 29, 2005
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES

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