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BIORETEC ACTIVASCREW INTERFERENCE

Bioretec, Ltd. · Class II · Cleared Aug 28, 2013

K-numberK130716
Device nameBIORETEC ACTIVASCREW INTERFERENCE
ApplicantBioretec, Ltd.
Product codeMAI
Device classClass II
Decision dateAug 28, 2013
DecisionSubstantially Equivalent
Regulation888.3030
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View the full FDA submission: accessdata.fda.gov

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