K-number	K925571
Device name	OTI EUROPEAN COMPRESSION SYSTEM
Applicant	Osteo-Technology Intl., Inc.
Product code	HRS
Device class	Class II
Decision date	Jul 13, 1993
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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OTI EUROPEAN COMPRESSION SYSTEM

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