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Dfine, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K091310 ABLATION INSTRUMENT, MODEL 1635; ABLATION MULTIPLEX CATHETER, MODEL 1682GEI2010-08-11 View
510(k) K090986 STABILI ERX BONE CEMENT, MODEL 1135,STABILIT VERTEBRAL AUGMENTATION SYSTEM (FOR USE W/ STABILIT ERX BONE CEMENT)NDN2009-12-30 View
510(k) K072496 MODIFICATION TO SPACE CPSXL BONE CEMENTNDN2007-10-05 View
510(k) K070351 SPACE 360 DELIVERY SYSTEMNDN2007-06-29 View
510(k) K061531 SPACE CPSXL BONE CEMENTNDN2006-08-30 View
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