K-number	K953664
Device name	VITALOCK SPIKED ACETABULAR SHELL
Applicant	Howmedica Corp.
Product code	LPH
Device class	Class II
Decision date	Oct 23, 1995
Decision	Substantially Equivalent
Regulation	888.3358

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View the full FDA submission: accessdata.fda.gov

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VITALOCK SPIKED ACETABULAR SHELL

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