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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