Osteomed Implantes, Ltda is one of 63 FDA 510(k) medical device manufacturers from Brazil in the dataset, ranked by real submission volume.
Osteomed Implantes, Ltda - FDA 510(k) Cleared Devices
Recent clearances: Anterior Cervical Plate System, Intersomatic Cervical Device - DICOM PEEK, Intersomatic Intervertebral Space Maintenance Device - DIMEI PEEK, Intersomatic Transforaminal - TLIF PEEK, DPZ Pedicular Fixation System
3
Total
3
Cleared
0
Denied
Osteomed Implantes, Ltda has 3 FDA 510(k) cleared medical devices. Based in Rio Claro - Sp, BR.
Historical record: 3 cleared submissions from 2015 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Osteomed Implantes, Ltda Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The OrthoMedix Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Osteomed Implantes, Ltda
3 devices