K-number	K012026
Device name	TRIDENT ALL POLY CUP
Applicant	Howmedica Osteonics Corp.
Product code	JDI
Device class	Class II
Decision date	Jul 18, 2001
Decision	Substantially Equivalent
Regulation	888.3350

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Source

View the full FDA submission: accessdata.fda.gov

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TRIDENT ALL POLY CUP

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