The following data is part of a premarket notification filed by Cardica, Inc. with the FDA for Modification To Cardica C-port Xa Distal Anastomosis System.
| Device ID | K090872 |
| 510k Number | K090872 |
| Device Name: | MODIFICATION TO CARDICA C-PORT XA DISTAL ANASTOMOSIS SYSTEM |
| Classification | Clip, Implantable |
| Applicant | CARDICA, INC. 900 SAGINAW DR. Redwood City, CA 94063 |
| Contact | Kimberlee Leon |
| Correspondent | Kimberlee Leon CARDICA, INC. 900 SAGINAW DR. Redwood City, CA 94063 |
| Product Code | FZP |
| CFR Regulation Number | 878.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-03-30 |
| Decision Date | 2009-04-21 |
| Summary: | summary |