FDA 510(k) Applications Submitted by Stefano Pullega

FDA 510(k) Number Submission Date Device Name Applicant
K180150 01/19/2018 PL8 Wrist Reconstruction Plate CITIEFFE S.r.l.
K150661 03/13/2015 ST.A.R. 90 F4 External Fixation Screws With Hydroxyapatite CITIEFFE s.r.l
K181540 06/11/2018 Estremo Citieffe Nailing System CITIEFFE S.r.L.
K163323 11/25/2016 Dolphix« External Fixation System MR Conditional CITIEFFE s.r.l
K183666 12/27/2018 EBA One Nailing System CITIEFFE S.r.l.


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