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FDA 510(k) Applications Submitted by G21 S.r.l
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190216
02/04/2019
SpaceFlex Knee
G21 S.R.L
K181282
05/15/2018
G3A 40 Bone Cement
G21 S.r.l
K201960
07/14/2020
SpaceFlex Knee - 80mm Size
G21 S.r.l
K192041
07/31/2019
G21 SpaceFlex Hip
G21 S.r.l
K193061
11/01/2019
G3 40 Radiopaque Bone Cement
G21 S.r.l
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