FDA 510(k) Applications Submitted by JOHN FERROS, SR.

FDA 510(k) Number Submission Date Device Name Applicant
K971189 04/01/1997 P.F.C. SIGMA KNEE SYSTEM (SIZE 1.5) JOHNSON & JOHNSON PROFESSIONALS, INC.
K971682 05/06/1997 J-FX CERCLAGE SYSTEM JOHNSON & JOHNSON PROFESSIONALS, INC.
K091626 06/03/2009 CRYOPATCH SG PULMONARY HEMI-ARTERY; TRUNK; BRANCH CRYOLIFE, INC.
K963885 09/26/1996 ULTIMA FX FEMORAL HIP STEMS JOHNSON & JOHNSON PROFESSIONALS, INC.
K963117 08/12/1996 P.F.C. CRUCIATE RETAING KNEE SYSTEM JOHNSON & JOHNSON PROFESSIONALS, INC.
K961685 05/01/1996 P.F.C. CRUCIATE RETAINING KNEE SYSTEM (SIZE 1.5) JOHNSON & JOHNSON PROFESSIONALS, INC.
K971652 05/06/1997 P.F.C. SIGMA INSET PATELLA JOHNSON & JOHNSON PROFESSIONALS, INC.
K952830 06/20/1995 DARWIN KNEE SYSTEM (TC3) JOHNSON & JOHNSON PROFESSIONALS, INC.
K101866 07/02/2010 CRYOPATCH SG PULMONARY HUMAN CARDIAC PATCH CRYOLIFE, INC.
K061892 07/03/2006 PROPATCH SOFT TISSUE REPAIR MATRIX CRYOLIFE, INC.
K092021 07/06/2009 CRYOVALVE SG PULMONARY HUMAN HEART VALVE (AND CONDUIT) CRYOLIFE, INC.
K083106 10/20/2008 CRYOVALVE SG PULMONARY VALVE AND CONDUIT CRYOLIFE, INC.
K955511 12/04/1995 ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR CUP JOINT MEDICAL PRODUCTS CORP.


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