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FDA 510(k) Applications Submitted by G21 S.R.L.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K193059
11/01/2019
G1 40 Radiopaque Bone Cement
G21 S.r.l.
K173494
11/13/2017
OrthoSteady G Bone Cement
G21 s.r.l.
K150408
02/18/2015
V-STEADY, V-FAST
G21 S.R.L.
K152557
09/08/2015
Winch Kyphoplasty(15 and 20 mm) 11 Gauge Balloon Catheters
G21 s.r.l.
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