K-number	K162800
Device name	BLUEPRINT Patient Specific Instrumentation
Applicant	Tornier S.A.S.
Product code	KWS
Device class	Class II
Decision date	Feb 22, 2017
Decision	Substantially Equivalent
Regulation	888.3660

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Source

View the full FDA submission: accessdata.fda.gov

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BLUEPRINT Patient Specific Instrumentation

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