510(k) K062170

BIOKNOTLESS AND LUPINE PLUS ANCHORS by Depuy Mitek, A Johnson & Johnson Company — Product Code JDR

K062170 is an FDA 510(k) premarket notification submitted by Depuy Mitek, A Johnson & Johnson Company for the device "BIOKNOTLESS AND LUPINE PLUS ANCHORS". The FDA issued a decision of Substantially Equivalent on Aug 22, 2006. The device falls under product code JDR (Staple, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Depuy Mitek, A Johnson & Johnson Company has 61 other 510(k) clearances on record.