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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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