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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact