K-number	K781389
Device name	BIOMET CONCENTRIC HEX SCREW
Applicant	Biomet, Inc.
Product code	JDO
Device class	Class II
Decision date	Aug 21, 1978
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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BIOMET CONCENTRIC HEX SCREW

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