K-number	K081067
Device name	FRACTURE/RECONSTRUCTION SYSTEM (TRAUMAONE)
Applicant	Biomet Microfixation, Inc.
Product code	JEY
Device class	Class II
Decision date	May 9, 2008
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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FRACTURE/RECONSTRUCTION SYSTEM (TRAUMAONE)

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