K-number	K082088
Device name	MAKO SURGICAL CORP. PATELLOFEMORAL KNEE IMPLANT SYSTEM II
Applicant	Mako Surgical Corp.
Product code	KRR
Device class	Class II
Decision date	Oct 22, 2008
Decision	Substantially Equivalent
Regulation	888.3540

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View the full FDA submission: accessdata.fda.gov

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MAKO SURGICAL CORP. PATELLOFEMORAL KNEE IMPLANT SYSTEM II

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