K-number	K994308
Device name	NUVASIVE TOWNLEY FACET SCREW
Applicant	Nuvasive, Inc.
Product code	MRW
Device class	Class U
Decision date	Apr 18, 2000
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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NUVASIVE TOWNLEY FACET SCREW

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