K-number	K853662
Device name	MUELLER CURVED STEM HEMI-PROSTHESIS
Applicant	Protek, Inc.
Product code	KWL
Device class	Class II
Decision date	Sep 24, 1985
Decision	Substantially Equivalent
Regulation	888.3360

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View the full FDA submission: accessdata.fda.gov

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MUELLER CURVED STEM HEMI-PROSTHESIS

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