FDA 510(k) Applications Submitted by MARC SEEGERS

FDA 510(k) Number Submission Date Device Name Applicant
K080101 01/14/2008 AAP CANNULATED SCREW AND DARCO HEADED SCREW AAP IMPLANTATE AG
K111316 05/10/2011 AAP CANNULATED SCREWS AAP IMPLANTATE AG
K121494 05/21/2012 LOQTEQ DISTAL LATERAL FEMUR PLATE 4.5 (LEFT AND RIGHT VERSION) LOQREQ CORTICAL SCREW 4.5 T25, SELF-TAPPING AAP IMPLANTATE AG
K121495 05/21/2012 LOQTEQ PROXIMAL HUMERUS PLATE 3.5, SHORT LOQTEQ PROXIMAL HUMERUS PLATE 3.5, LONG AAP IMPLANTATE AG
K071852 07/05/2007 AAP APS SYSTEM AAP IMPLANTATE AG
K072411 08/27/2007 AAP BONE PLATES AND SCREW IMPLANTS AAP IMPLANTATE AG
K033260 10/09/2003 AEQUOS AAP IMPLANTATE AG
K113601 12/05/2011 AAP LOQTEQ DISTAL MEDIAL TIBIA PLATE 3.5 SYSTEM AAP IMPLANTATE AG
K113602 12/05/2011 AAP LOQTEQ PROXIMAL LATERAL TIBIA PLATE 4.5 SYSTEM AAP IMPLANTATE AG
K113648 12/12/2011 LOQTEQ LARGE FRAGMENT SET LOQTEQ CORTICAL SCREW 4.5, SMALL HEAD, T25, SELF TAPPING LOQTEQ CORTICAL SCREW 4.5, T25, SELF AAP IMPLANTATE AG
K113652 12/12/2011 LOQTEQ SMALL FRAGMENT SET LOQTEQ CORTICAL SCREW3.5, SMALL HEAD, T15, SELF TAPPING LOQTEQ CORTICAL SCREW 3.5, T15, SELF T AAP IMPLANTATE AG


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