K-number	K081244
Device name	LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS
Applicant	Biomet Trauma
Product code	KTT
Device class	Class II
Decision date	Jul 30, 2008
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS

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