K-number	K102438
Device name	PRIMALOK FACET FIXATION SYSTEM
Applicant	Osteomed LP
Product code	MRW
Device class	Class U
Decision date	Sep 30, 2010
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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PRIMALOK FACET FIXATION SYSTEM

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