K-number	K052871
Device name	STRYKER CUSTOM TI IMPLANT
Applicant	Stryker Leibinger
Product code	GXN
Device class	Class II
Decision date	Dec 16, 2005
Decision	Substantially Equivalent
Regulation	882.5330

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View the full FDA submission: accessdata.fda.gov

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STRYKER CUSTOM TI IMPLANT

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