K-number	K133354
Device name	PERI-PROSTHETIC CABLE SYSTEM
Applicant	Biomet, Inc.
Product code	JDQ
Device class	Class II
Decision date	Jan 27, 2014
Decision	Substantially Equivalent
Regulation	888.3010

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Source

View the full FDA submission: accessdata.fda.gov

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PERI-PROSTHETIC CABLE SYSTEM

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