FDA 510(k) Applications Submitted by Ritter Implants GmbH & Co. KG

FDA 510(k) Number Submission Date Device Name Applicant
K180183 01/23/2018 Ritter Dental Implant System Ritter Implants GmbH & Co. KG
K160475 02/19/2016 Ritter Dental Implant System Ritter Implants GmbH & Co. KG


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