K-number	K091913
Device name	HI TECH IMPLANT, HT PHYSIO IMPLANT
Applicant	By Dental Srl
Product code	EKX
Device class	Class I
Decision date	Oct 30, 2009
Decision	Substantially Equivalent
Regulation	872.4200

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View the full FDA submission: accessdata.fda.gov

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HI TECH IMPLANT, HT PHYSIO IMPLANT

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