Orthospin is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Orthospin - FDA 510(k) Cleared Devices
Recent clearances: AutoStrut
1
Total
1
Cleared
0
Denied
Orthospin has 1 FDA 510(k) cleared medical devices. Based in Misgav, IL.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthospin Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US Lpp as regulatory consultant.
FDA 510(k) Regulatory Record - Orthospin
1 devices