K-number	K003077
Device name	SMARTSCREW MODEL 222006...227510
Applicant	Bionx Implants, Ltd.
Product code	HWC
Device class	Class II
Decision date	Apr 26, 2001
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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SMARTSCREW MODEL 222006...227510

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