FDA 510(k) Applications Submitted by Clariance SAS

FDA 510(k) Number Submission Date Device Name Applicant
K183259 11/21/2018 IdysÖ TLIF TiVac Clariance SAS
K191263 05/10/2019 Idys ALIF TiVac Clariance SAS
K170163 01/18/2017 Erisma« LP Spinal Fixation System CLARIANCE SAS
K172083 07/10/2017 IdysÖ ALIF System CLARIANCE SAS
K162367 08/23/2016 Erisma« LP MIS CLARIANCE SAS


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