FDA 510(k) Applications Submitted by CHRISTIAN ZIETSCH

FDA 510(k) Number Submission Date Device Name Applicant
K130590 03/07/2013 AAP CANNULATED SCREW 2.0 AAP IMPLANTATE AG
K140607 03/10/2014 AAP LOQTEC(R) OLECRANON PLATE AAP IMPLANTATE AG
K150974 04/13/2015 aap Cortical Screw 1.5, self-tapping, aap Cortical Screw 1.5, self-tapping, Titanium AAP IMPLANTATE AG
K131459 05/20/2013 AAP K-WIRE, STEINMANN PIN, CERCLAGE WIRE AAP IMPLANTATE AG
K131782 06/17/2013 LOQTEQ HIGH TIBIA OSTEOTOMY PLATE 4.5 AAP IMPLANTATE AG
K141823 07/07/2014 AAP LOQTEC CLAVICLE PLATES 2.7/3.5 AAP IMPLANTATE AG
K141949 07/18/2014 CORTICAL SCREW 3.5, T15, SELF-TAPPING, TITANIUM, CORTICAL SCREW 4.5, T25, SELF TAPPING, TITANIUM AAP IMPLANTATE AG
K132554 08/14/2013 AAP LOQTEQ PROXIMAL MEDIAL TIBIA PLATE 3.5 AAP IMPLANTATE AG
K132787 09/06/2013 LOQTEQ DISTAL DORSOLATERAL HUMERUS PLATE AAP IMPLANTATE AG
K153034 10/19/2015 aap LOQTEQ VA Radius Set 2.5 AAP IMPLANTATE AG
K133675 11/29/2013 AAP LOQTEQ DISTAL ANTEROLATERAL TIBIA PLATE 3.5 AAP IMPLANTATE AG
K123875 12/17/2012 AAP RADIUS SET 2.5 AAP IMPLANTATE AG


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