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FDA 510(k) Applications Submitted by Berny Villejeune
FDA 510(k) Number
Submission Date
Device Name
Applicant
K242141
07/22/2024
TiLink-P SI Joint Fusion System
SurGenTec, LLC
K243835
12/13/2024
TiLink-P SI Joint Fusion System
SurGenTec LLC
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