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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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