K-number	K140898
Device name	PATIENT SPECIFIC DISTAL FEMORAL
Applicant	Stanmore Implants Worldwide , Ltd.
Product code	KRO
Device class	Class II
Decision date	Jan 20, 2015
Decision	Substantially Equivalent
Regulation	888.3510

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Source

View the full FDA submission: accessdata.fda.gov

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PATIENT SPECIFIC DISTAL FEMORAL

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