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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