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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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