510(k) K041115

GII QUICKANCHOR PLUS by Depuy Mitek, A Johnson & Johnson Company — Product Code JDR

K041115 is an FDA 510(k) premarket notification submitted by Depuy Mitek, A Johnson & Johnson Company for the device "GII QUICKANCHOR PLUS". The FDA issued a decision of Substantially Equivalent on May 28, 2004. 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.