FDA 510(k) Applications Submitted by ACKERMANN INSTRUMENTE GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K974382 | 11/21/1997 | ACKERMANN SURGICAL INSTRUMENTS | ACKERMANN INSTRUMENTE GMBH |
| K111930 | 07/07/2011 | ACKERMANN EUROPCLIP | ACKERMANN INSTRUMENTE GMBH |
| K143450 | 12/02/2014 | Ackermann Intervertebral Body Fusion Device | ACKERMANN INSTRUMENTE GMBH |
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