FDA approves device for treatment of osteoid osteoma in the extremities

Food and Drug Administration approved the Sonalleve MR-HIFU system (Profound Medical Inc.) for the treatment of osteoid osteoma in the extremities. November 27, 2020.  More Information: https://www.gov/drugs/drug-approvals-and-databases/fda-approves-device-treatment-osteoid-osteoma-extremities Manage Subscriptions  |  Unsubscribe All  |  Help This email was sent to ooseims.archieves@blogger.com using GovDelivery Communications Cloud on behalf of: U.S. Food and Drug Administration ·  10903 New Hampshire Ave · Silver Spring, MD ·  20993-0002 ·  1-888-INFO-FDA