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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