Orthospin, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Orthospin, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Yokneam, IL.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthospin, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Orthospin, Ltd.
1 devices