K-number	K071851
Device name	HDC STERILE SPIDER SCREW
Applicant	Hdc S.R.L.
Product code	DZE
Device class	Class II
Decision date	Oct 18, 2007
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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HDC STERILE SPIDER SCREW

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