K-number	K112301
Device name	ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNER
Applicant	Materialise NV
Product code	HSX
Device class	Class II
Decision date	Jan 6, 2012
Decision	Substantially Equivalent
Regulation	888.3520

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Source

View the full FDA submission: accessdata.fda.gov

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ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNER

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