K-number	K061253
Device name	REFLECTION 3 ACETABULAR SYSTEM
Applicant	Smith & Nephew, Inc.
Product code	MBL
Device class	Class II
Decision date	May 31, 2006
Decision	Substantially Equivalent
Regulation	888.3358

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Source

View the full FDA submission: accessdata.fda.gov

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REFLECTION 3 ACETABULAR SYSTEM

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