K-number	K990920
Device name	DRG TITANIUM BONE PLATE
Applicant	Doctor'S Research Group, Inc.
Product code	JEY
Device class	Class II
Decision date	Jun 10, 1999
Decision	Substantially Equivalent
Regulation	872.4760

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View the full FDA submission: accessdata.fda.gov

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DRG TITANIUM BONE PLATE

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