K-number	K081575
Device name	HU/HS/HG PROSTHETIC SYSTEM
Applicant	Osstem Implant Co., Ltd.
Product code	NHA
Device class	Class II
Decision date	Sep 2, 2008
Decision	Substantially Equivalent
Regulation	872.3630

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View the full FDA submission: accessdata.fda.gov

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HU/HS/HG PROSTHETIC SYSTEM

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