K-number	K030302
Device name	HBS HEADLESS BONE SCREW
Applicant	Schoening & Assoc., Inc.
Product code	HWC
Device class	Class II
Decision date	Aug 8, 2003
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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HBS HEADLESS BONE SCREW

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