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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