K-number	K943474
Device name	CANNULATED BONE SCREW
Applicant	Cohort Medical Products Group, Inc.
Product code	HWC
Device class	Class II
Decision date	Oct 14, 1994
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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CANNULATED BONE SCREW

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