K-number	K920193
Device name	OMNIFLEX M-HA HIP STEM SERIES
Applicant	Stryker Corp.
Product code	KWL
Device class	Class II
Decision date	Jun 8, 1992
Decision	Substantially Equivalent
Regulation	888.3360

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View the full FDA submission: accessdata.fda.gov

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OMNIFLEX M-HA HIP STEM SERIES

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