Dfine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ABLATION INSTRUMENT, MODEL 1635, STABILI ERX BONE CEMENT, MODEL 1135,STABILIT VERTEBRAL AUGMENTATION SYSTEM (FOR USE W/ STABILIT ERX BONE CEMENT), MODIFICATION TO SPACE CPSXL BONE CEMENT
5
Total
5
Cleared
0
Denied