K-number	K090786
Device name	KENS INTERNAL FIXATION SYSTEM
Applicant	Kens Finemedtech Sdn. Bhd
Product code	HRS
Device class	Class II
Decision date	Jun 18, 2009
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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KENS INTERNAL FIXATION SYSTEM

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