Ossur Americans (Formerly the Jerome Group) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ossur Americans (Formerly the Jerome Group) - FDA 510(k) Cleared Devi...
1
Total
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Cleared
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Denied
Ossur Americans (Formerly the Jerome Group) has 1 FDA 510(k) cleared medical devices. Based in Paulsboro, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Ossur Americans (Formerly the Jerome Group) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ossur Americans (Formerly the Jerome Group)
1 devices