FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MODIFICATION TO CARDICA C-PORT XA DISTAL ANASTOMOSIS SYSTEM

K Number: K090872 · Decision Apr 21, 2009
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
175
Applicant Total
15
Review Days
22

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Basic Information

Device Name
MODIFICATION TO CARDICA C-PORT XA DISTAL ANASTOMOSIS SYSTEM
K Number
K090872
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardica, Inc.
Date Received
March 30, 2009
Decision Date
April 21, 2009
Product Code
FZP
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FZP Clip, Implantable

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Other Clearances by Cardica, Inc.

K Number Device Name
K161137 Dextera MicroCutter 5/80 Blue Reload, Dextera MicroCutter 5/80 Blue Curved Tip Reload
K151081 MicroCutter XCHANGE 30 Stapler, MicroCutter XCHANGE 30 Blue Cartridge, MicroCutter XCHANGE 30 White Cartridge
K140118 MICROCUTTER XCHANGE 30 STAPLER, MICROCUTTER XCHANGE 30 BLUE CARTRIDGE
K140170 MICROCUTTER XCHANGE 30 STAPLER, MICROCUTTER XCHANGE 30 WHITE CARTRIDGE
K132581 MICROCUTTER XCHANGE 30, MICROCUTTER XCHANGE 30, BLUE STAPLE CARTRIDGE, BLUE STAPLE CARTRIDGE
K101018 CARDICA C-PORT XA PLUS DISTAL ANASTOMOSIS SYSTEM, MODEL FG-000100
K091017 CARDICA PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM, MODEL FG-000001
K081225 CARDICA PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM
K073304 CARDICA C-PORT X-CHANGE ANASTOMOSIS SYSTEM AND HANDLE AND XA X-CHANGE SUBASSEMBLIES
K073123 CARDICA C-PORT FLEX-A DISTAL ANASTOMOSIS SYSTEM, MODEL FG-000150
Search all 15 clearances from Cardica, Inc. →