K-number	K882671
Device name	SAMUELSON SCREWLOC CUP
Applicant	Protek, Inc.
Product code	KWA
Device class	Class III
Decision date	Oct 20, 1988
Decision	Substantially Equivalent
Regulation	888.3330

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View the full FDA submission: accessdata.fda.gov

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SAMUELSON SCREWLOC CUP

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