K-number	K073465
Device name	US/GS ULTRA WIDE SYSTEM
Applicant	Osstem Implant Co., Ltd.
Product code	DZE
Device class	Class II
Decision date	Apr 7, 2008
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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US/GS ULTRA WIDE SYSTEM

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