K-number	K070179
Device name	TROKABONE, TROKABONE STERNAL
Applicant	PAJUNK GmbH Medizintechnologie
Product code	FCG
Device class	Class II
Decision date	Mar 7, 2007
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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TROKABONE, TROKABONE STERNAL

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