FDA 510(k) Applications Submitted by FABIO VON ZEPPELIN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121253 | 04/25/2012 | MERIDIAN CRANIAL PERFORATOR | ADEOR MEDICAL TECHNOLOGIES GMBH |
| K130755 | 03/19/2013 | HICUT HIGHSPEED INSTRUMENT | ADEOR MEDICAL AG |
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