K-number	K024125
Device name	HALM ZIELKE INSTRUMENTATION SYSTEM
Applicant	Micomed Ortho GmbH
Product code	KWQ
Device class	Class II
Decision date	Sep 22, 2003
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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HALM ZIELKE INSTRUMENTATION SYSTEM

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