G-21 S.R.L. is one of 221 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
G-21 S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: Modified Winch Kyphoplasty (15 and 20 mm) 11 Gauge Balloon Catheters
1
Total
1
Cleared
0
Denied
G-21 S.R.L. has 1 FDA 510(k) cleared medical devices. Based in San Possidonio, IT.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by G-21 S.R.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQMIS, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - G-21 S.R.L.
1 devices