K-number	K030492
Device name	TITANIUM OSSICULAR REPLACMENT SYSTEM
Applicant	Invotec International, Inc.
Product code	ETA
Device class	Class II
Decision date	Mar 3, 2003
Decision	Substantially Equivalent
Regulation	874.3495

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View the full FDA submission: accessdata.fda.gov

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TITANIUM OSSICULAR REPLACMENT SYSTEM

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