FDA 510(k) Applications Submitted by DENISE LUCIANO

FDA 510(k) Number Submission Date Device Name Applicant
K050771 03/25/2005 LUPINE LOOP DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K051989 07/22/2005 GII QUICKANCHOR PLUS WITH ORTHOCORD SUTURE DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K052630 09/26/2005 ROTATOR CUFF QUICKANCHOR PLUS (WITH ORTHOCORD SUTURE) DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K052631 09/26/2005 SUPER QUICKANCHOR PLUS (WITH ORTHOCORD SUTURE) DEPUY MITEK, A JOHNSON & JOHNSON COMPANY


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