K-number	K030312
Device name	PORTA IMPLANT
Applicant	Wieland Dental + Technik GmbH & Co. KG
Product code	EJT
Device class	Class II
Decision date	Mar 26, 2003
Decision	Substantially Equivalent
Regulation	872.3060

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View the full FDA submission: accessdata.fda.gov

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PORTA IMPLANT

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