FDA 510(k) Applications Submitted by BRIAN S ZIMOVAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K093086 | 10/01/2009 | ARTHROSTEER ABLATOR & COAGULATOR, MODELS: REF 1070 & 1080 | ORTHODYNAMIX, LLC |
| K034029 | 12/29/2003 | TI CLIP APPLIER | GYRX, LLC |
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