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FDA 510(k) Applications Submitted by ZIMMER MEDIZINSYSTEMS GMBH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K121059
04/06/2012
SOLEOLINE, SOLEO STIM, SOLEO SONO, SOLEO SONOSTIM
ZIMMER MEDIZINSYSTEMS GMBH
K141564
06/12/2014
OPTON PRO
ZIMMER MEDIZINSYSTEMS GMBH
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