K-number	K093983
Device name	SMPLE PLATE AND SCREWS
Applicant	Biomet Trauma (Aka Ebi, Lp)
Product code	HRS
Device class	Class II
Decision date	Mar 19, 2010
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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SMPLE PLATE AND SCREWS

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