K-number	K110787
Device name	TRIPORE TDD (HA), TRIPORE TDD (BP90), TRIPORE TDD (BP15)
Applicant	Orthogem Limited
Product code	MQV
Device class	Class II
Decision date	Apr 21, 2011
Decision	Substantially Equivalent
Regulation	888.3045

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Source

View the full FDA submission: accessdata.fda.gov

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TRIPORE TDD (HA), TRIPORE TDD (BP90), TRIPORE TDD (BP15)

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