K-number	K010367
Device name	MODIFICATION TO TITANIUM TRI-LOCK HIPS STEM
Applicant	DePuy Orthopaedics, Inc.
Product code	LPH
Device class	Class II
Decision date	Mar 9, 2001
Decision	Substantially Equivalent
Regulation	888.3358

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO TITANIUM TRI-LOCK HIPS STEM

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