K-number	K800207
Device name	UHR UNIVERSAL6HIP REPLACEMENT
Applicant	Osteonics Corp.
Product code	KWL
Device class	Class II
Decision date	Feb 11, 1980
Decision	Substantially Equivalent
Regulation	888.3360

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View the full FDA submission: accessdata.fda.gov

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UHR UNIVERSAL6HIP REPLACEMENT

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