K-number	K010515
Device name	MODIFICATION TO SYNERGY SPINAL SYSTEM
Applicant	Interpore Cross Intl.
Product code	KWP
Device class	Class II
Decision date	Mar 22, 2001
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO SYNERGY SPINAL SYSTEM

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