K-number	K043250
Device name	STRYKER PATIENT SPECIFIC POLYMER IMPLANT
Applicant	Stryker Leibinger
Product code	KKY
Device class	Class II
Decision date	Apr 15, 2005
Decision	Substantially Equivalent
Regulation	878.3500

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Source

View the full FDA submission: accessdata.fda.gov

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STRYKER PATIENT SPECIFIC POLYMER IMPLANT

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