Cardica, Inc. is one of 4771 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardica, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Cardica, Inc. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Redwood City, US.
Historical record: 15 cleared submissions from 2005 to 2016.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardica, Inc.
15 devices
Cleared
Jul 20, 2016
Dextera MicroCutter 5/80 Blue Reload, Dextera MicroCutter 5/80 Blue Curved...
General & Plastic Surgery
89d
Cleared
Jan 15, 2016
MicroCutter XCHANGE 30 Stapler, MicroCutter XCHANGE 30 Blue Cartridge,...
General & Plastic Surgery
268d
Cleared
Feb 25, 2014
MICROCUTTER XCHANGE 30 STAPLER, MICROCUTTER XCHANGE 30 BLUE CARTRIDGE
General & Plastic Surgery
40d
Cleared
Feb 19, 2014
MICROCUTTER XCHANGE 30 STAPLER, MICROCUTTER XCHANGE 30 WHITE CARTRIDGE
General & Plastic Surgery
27d
Cleared
Jan 07, 2014
MICROCUTTER XCHANGE 30, MICROCUTTER XCHANGE 30, BLUE STAPLE CARTRIDGE, BLUE...
General & Plastic Surgery
144d
Cleared
Jun 25, 2010
CARDICA C-PORT XA PLUS DISTAL ANASTOMOSIS SYSTEM, MODEL FG-000100
General & Plastic Surgery
73d
Cleared
Apr 29, 2009
CARDICA PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM, MODEL FG-000001
General & Plastic Surgery
20d
Cleared
Apr 21, 2009
MODIFICATION TO CARDICA C-PORT XA DISTAL ANASTOMOSIS SYSTEM
General & Plastic Surgery
22d
Cleared
Sep 05, 2008
CARDICA PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM
General & Plastic Surgery
128d
Cleared
Dec 20, 2007
CARDICA C-PORT X-CHANGE ANASTOMOSIS SYSTEM AND HANDLE AND XA X-CHANGE...
General & Plastic Surgery
27d
Cleared
Dec 06, 2007
CARDICA C-PORT FLEX-A DISTAL ANASTOMOSIS SYSTEM, MODEL FG-000150
General & Plastic Surgery
30d
Cleared
Mar 29, 2007
C-PORT FLEXA DISTAL ANASTOMOSIS SYSTEM
General & Plastic Surgery
31d