K-number	K872019
Device name	BI-ARTICULAR II HIP DEVICE
Applicant	Zimmer, Inc.
Product code	KWY
Device class	Class II
Decision date	Jul 21, 1987
Decision	Substantially Equivalent
Regulation	888.3390

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View the full FDA submission: accessdata.fda.gov

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BI-ARTICULAR II HIP DEVICE

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