FDA 510(k) Applications Submitted by MICOMED ORTHO GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K024125 | 12/16/2002 | HALM ZIELKE INSTRUMENTATION SYSTEM | MICOMED ORTHO GMBH |
| K021275 | 04/22/2002 | MICOMED POSTERIOR DOUBLEROD SYSTEM | MICOMED ORTHO GMBH |
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