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FDA 510(k) Applications Submitted by CITIEFFE S.r.l.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K131005
04/11/2013
EBA2 FEMORAL NAILING SYSTEM
CITIEFFE S.R.L.
K132363
07/30/2013
DOLPHIX EXTERNAL FIXATION SYSTEM
CITIEFFE S.R.L.
K180150
01/19/2018
PL8 Wrist Reconstruction Plate
CITIEFFE S.r.l.
K181540
06/11/2018
Estremo Citieffe Nailing System
CITIEFFE S.r.L.
K183666
12/27/2018
EBA One Nailing System
CITIEFFE S.r.l.
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