K-number	K130402
Device name	SPIDER SYSTEM KOLIBRI CEMENT NEEDLE
Applicant	Sintea Plustek, LLC
Product code	NDN
Device class	Class II
Decision date	Apr 1, 2013
Decision	Substantially Equivalent
Regulation	888.3027

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Source

View the full FDA submission: accessdata.fda.gov

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SPIDER SYSTEM KOLIBRI CEMENT NEEDLE

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