K-number	K050497
Device name	BIOSCREW XTRALOK, 8X35MM & 8X40MM VIOLET
Applicant	Linvatec Corp.
Product code	HWC
Device class	Class II
Decision date	Mar 25, 2005
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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BIOSCREW XTRALOK, 8X35MM & 8X40MM VIOLET

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