K-number	K970713
Device name	COMPASS UNIVERSAL HINGE
Applicant	Smith & Nephew, Inc., Orthopaedic Div.
Product code	JDW
Device class	Class II
Decision date	Apr 3, 1997
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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COMPASS UNIVERSAL HINGE

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