K-number	K062553
Device name	SIMPLEX P BONE CEMENT
Applicant	Stryker Orthopaedics
Product code	LOD
Device class	Class II
Decision date	Jan 8, 2007
Decision	Substantially Equivalent
Regulation	888.3027

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View the full FDA submission: accessdata.fda.gov

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SIMPLEX P BONE CEMENT

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