K-number	K140622
Device name	DVR DORSAL PLATE, DVR LATERAL PLATE, DVR ULNA PLATE
Applicant	Biomet, Inc.
Product code	HRS
Device class	Class II
Decision date	May 13, 2014
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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DVR DORSAL PLATE, DVR LATERAL PLATE, DVR ULNA PLATE

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