K-number	K013312
Device name	P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)
Applicant	Spine Vision, Inc.
Product code	KWP
Device class	Class II
Decision date	Feb 13, 2002
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)

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