K-number	K153398
Device name	Comprehensive SRS/Nexel Elbow
Applicant	Biomet Manufacturing Corp
Product code	JDC
Device class	Class II
Decision date	Feb 3, 2016
Decision	Substantially Equivalent
Regulation	888.3150

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Source

View the full FDA submission: accessdata.fda.gov

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Comprehensive SRS/Nexel Elbow

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