K-number	K083073
Device name	THEKEN ATOLL CERVICO-THORACIC SYSTEM
Applicant	Theken Spine, LLC
Product code	MNI
Device class	Class II
Decision date	Mar 13, 2009
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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THEKEN ATOLL CERVICO-THORACIC SYSTEM

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