K-number	K121682
Device name	ACTIVE SCREW BONE SCREW
Applicant	Intelligent Implant Systems, LLC
Product code	HWC
Device class	Class II
Decision date	Oct 4, 2012
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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ACTIVE SCREW BONE SCREW

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