K-number	K132373
Device name	BIOMET ACCESS SYSTEM
Applicant	Biomet Spine (Aka Ebi, LLC)
Product code	PDQ
Device class	Class II
Decision date	Mar 27, 2014
Decision	Substantially Equivalent
Regulation	874.1820

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Source

View the full FDA submission: accessdata.fda.gov

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BIOMET ACCESS SYSTEM

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