K-number	K093533
Device name	ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, VERSION 2.0
Applicant	Materialise NV
Product code	MBH
Device class	Class II
Decision date	Feb 17, 2010
Decision	Substantially Equivalent
Regulation	888.3565

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View the full FDA submission: accessdata.fda.gov

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ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, VERSION 2.0

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