K-number	K954213
Device name	ATH FULL PROFILE ACETABULAR CUP SYSTEM
Applicant	Kinamed, Inc.
Product code	LPH
Device class	Class II
Decision date	Oct 25, 1995
Decision	Substantially Equivalent
Regulation	888.3358

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View the full FDA submission: accessdata.fda.gov

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ATH FULL PROFILE ACETABULAR CUP SYSTEM

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