FDA 510(k) Applications Submitted by JENIK RADON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K050457 | 02/23/2005 | MERETE METAFIX SMALL FRAGMENT BONE PLATE SYSTEM | MERETE MEDICAL GMBH |
| K050924 | 04/13/2005 | MERETE DUOTHREADTM BONE SCREW | MERETE MEDICAL GMBH |
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