K-number	K122737
Device name	GEMINUS FOSSA SPECIFIC PLATE SYSTEM
Applicant	Skeletal Dynamics, LLC
Product code	HRS
Device class	Class II
Decision date	Oct 3, 2012
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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GEMINUS FOSSA SPECIFIC PLATE SYSTEM

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