K-number	K000683
Device name	MODIFIED SINGLE AXLE TOTAL ELBOW
Applicant	Biomet, Inc.
Product code	JDC
Device class	Class II
Decision date	Jun 27, 2000
Decision	Substantially Equivalent
Regulation	888.3150

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View the full FDA submission: accessdata.fda.gov

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MODIFIED SINGLE AXLE TOTAL ELBOW

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