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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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