510(k) Report

510(k) · Cleared

Recalled · Class II · 2018

Cardica C-Port XA Distal Anastomosis System

K063644510(k) SpecialCleared Jan 11, 200735-day reviewClass II21 CFR 878.4300Recalls 1

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Cardica, Inc. · FZP Clip, Implantable

Cleared on Jan 11, 2007 as substantially equivalent to K053524 (Cardica, Inc., 2006) and 1 other predicate after a 35-day review. Its family tree reaches back 11 generations to 1993. 5 later devices descend from it. It has been recalled once.

Decided
Jan 11, 2007
Review
35 days
Class
Class II
Product code
FZP
Recalls
1
Predicates
2

Its longest line of descent runs back 11 generations to K933887 (1993). 34 ancestors in all, the oldest K771412 (1977). 5 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 1 other ancestor2000: 2 other ancestors1998: 2 other ancestors1997: 3 other ancestors1996: 2 other ancestors1994: 3 other ancestors1991: 1 other ancestor1989: 1 other ancestor1984: 1 other ancestor1982: 1 other ancestor1977: 1 other ancestor2001: 1 other ancestor1995: 3 other ancestors1992: 1 other ancestor2009: 1 descendant cleared2007: 3 descendants cleared2010: 1 descendant clearedK933887 · Implantable Clip · United States Surgical, A Division of Tyco Healthc · 1993K962043 · Auto Suture Modified VCS Clip Applier · United States Surgical, A Division of Tyco Healthc · 1996 · recalledK994160 · Coalescent Surgical Sutured-Clip · Coalescent Surgical · 2000×6: 6 generations cleared close together, K012317 (2001), K013664 (2002), K021407 (2002), K023125 (2002), K024366 (2003), K031623 (2003) K040832 · C-Port Anastomosis System (Deployment System, Clip, Accessories), Model FG-000050 · Cardica, Inc. · 2005K053524 · C-Port Distal Anastomosis System · Cardica, Inc. · 2006 · recalled19801990200020102020
  1. Root · 11 generations backK933887 Implantable ClipUnited States Surgical, A Division of Tyco Healthc · 1993
  2. 7 generations between
  3. 3 generations backK031623 Modification to Coalescent Surgical U-Clip and AccessoriesCoalescent Surgical · 2003 · Recalled
  4. 2 generations backK040832 C-Port Anastomosis System (Deployment System, Clip, Accessories)…Cardica, Inc. · 2005
  5. 1 generation backK053524 C-Port Distal Anastomosis SystemCardica, Inc. · 2006 · Recalled
  6. This deviceK063644 Cardica C-Port XA Distal Anastomosis SystemCardica, Inc. · 2007
  7. Descendant · cites it directly · 1 of its ownK090872 Modification to Cardica C-Port XA Distal Anastomosis SystemCardica, Inc. · 2009 · Recalled
  8. Descendant · cites it directly · 1 of its ownK070548 C-Port Flexa Distal Anastomosis SystemCardica, Inc. · 2007 · Recalled
  9. Descendant · 2 generations on · 0 of its ownK101018 Cardica C-Port XA Plus Distal Anastomosis System, Model FG-000100Cardica, Inc. · 2010 · Recalled
  10. Descendant · cites it directly · 0 of its ownK073304 Cardica C-Port X-Change Anastomosis System and Handle and XA…Cardica, Inc. · 2007
  11. Descendant · 2 generations on · 0 of its ownK073123 Cardica C-Port Flex-a Distal Anastomosis System, Model FG-000150Cardica, Inc. · 2007 · Recalled
Show all 11 generations
  1. Root · 11 generations backK933887 Implantable ClipUnited States Surgical, A Division of Tyco Healthc · 1993
  2. 10 generations backK962043 Auto Suture Modified VCS Clip ApplierUnited States Surgical, A Division of Tyco Healthc · 1996 · Recalled
  3. 9 generations backK994160 Coalescent Surgical Sutured-ClipCoalescent Surgical · 2000
  4. 8 generations backK012317 Coalescent Surgical U-ClipCoalescent Surgical · 2001
  5. 7 generations backK013664 Coalescent Surgical U-ClipCoalescent Surgical · 2002
  6. 6 generations backK021407 Coalescent Surgical U-Clip - or Other TBD and AccessoriesCoalescent Surgical · 2002
  7. 5 generations backK023125 Coalescent U-Clip- and AccessoriesCoalescent Surgical · 2002
  8. 4 generations backK024366 Coalescent Surgical U-Clip and AccessoriesCoalescent Surgical · 2003 · Recalled
  9. 3 generations backK031623 Modification to Coalescent Surgical U-Clip and AccessoriesCoalescent Surgical · 2003 · Recalled
  10. 2 generations backK040832 C-Port Anastomosis System (Deployment System, Clip, Accessories)…Cardica, Inc. · 2005
  11. 1 generation backK053524 C-Port Distal Anastomosis SystemCardica, Inc. · 2006 · Recalled
  12. This deviceK063644 Cardica C-Port XA Distal Anastomosis SystemCardica, Inc. · 2007

Most influential descendants

Showing 5 of 5 · See all
  • K090872Modification to Cardica C-Port XA Distal Anastomosis SystemCardica, Inc. · 2009 · cites it directly1descendant
  • K070548C-Port Flexa Distal Anastomosis SystemCardica, Inc. · 2007 · cites it directly1descendant
  • K101018Cardica C-Port XA Plus Distal Anastomosis System, Model FG-000100Cardica, Inc. · 2010 · 2 generations on0descendants
  • K073304Cardica C-Port X-Change Anastomosis System and Handle and XA X-Change SubassembliesCardica, Inc. · 2007 · cites it directly0descendants
  • K073123Cardica C-Port Flex-a Distal Anastomosis System, Model FG-000150Cardica, Inc. · 2007 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K933887Implantable ClipUnited States Surgical, A Division of Tyco Healthc1993—
−10K962043Auto Suture Modified VCS Clip ApplierUnited States Surgical, A Division of Tyco Healthc19967
−9K994160Coalescent Surgical Sutured-ClipCoalescent Surgical2000—
−8K012317Coalescent Surgical U-ClipCoalescent Surgical2001—
−7K013664Coalescent Surgical U-ClipCoalescent Surgical2002—
−6K021407Coalescent Surgical U-Clip - or Other TBD and AccessoriesCoalescent Surgical2002—
−5K023125Coalescent U-Clip- and AccessoriesCoalescent Surgical2002—
−4K024366Coalescent Surgical U-Clip and AccessoriesCoalescent Surgical20031
−3K031623Modification to Coalescent Surgical U-Clip and AccessoriesCoalescent Surgical20034
−2K040832C-Port Anastomosis System (Deployment System, Clip, Accessories), Model…Cardica, Inc.2005—
−1K053524C-Port Distal Anastomosis SystemCardica, Inc.20061
0 (this device)K063644Cardica C-Port XA Distal Anastomosis SystemCardica, Inc.2007—
+1K090872Modification to Cardica C-Port XA Distal Anastomosis SystemCardica, Inc.20091
+1K070548C-Port Flexa Distal Anastomosis SystemCardica, Inc.20071
+2K101018Cardica C-Port XA Plus Distal Anastomosis System, Model FG-000100Cardica, Inc.20101
+1K073304Cardica C-Port X-Change Anastomosis System and Handle and XA X-Change…Cardica, Inc.2007—
+2K073123Cardica C-Port Flex-a Distal Anastomosis System, Model FG-000150Cardica, Inc.20071

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197710
198210
198410
198910
199110
199210
199430
199530
199620
199730
199820
200020
200110
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200730
200910
201010
FIG. 1 — Lineage of K063644, 1993–2010Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FZP? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new FZP device

  1. #1 K260677 Vessel Closure Device (VCD177213P)score 12.6 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K053524C-Port Distal Anastomosis System
Summary page 1
…tomosis System Common Name: Cardiovascular Surgical Instruments Predicate Device(s) Cardica® C-Podt xA Anastomosis System (K053524) Cardica® C-Pod® Anastomosis System (K040832) Device Description The Cardica C-Port xA Anasto…
Cardica, Inc.20061
*K040832C-Port Anastomosis System (Deployment System, Clip, Accessories), Model FG-000050
Summary page 1
…ovascular Surgical Instruments Predicate Device(s) Cardica® C-Podt xA Anastomosis System (K053524) Cardica® C-Pod® Anastomosis System (K040832) Device Description The Cardica C-Port xA Anastomosis System is a sterile, single use device…
Cardica, Inc.2005—

Also cleared against K053524: 1 other device →

What descends from it? (5)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K090872Modification to Cardica C-Port XA Distal Anastomosis SystemCardica, Inc.20091
K070548C-Port Flexa Distal Anastomosis SystemCardica, Inc.20071
K073304Cardica C-Port X-Change Anastomosis System and Handle and XA X-Change SubassembliesCardica, Inc.20070

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Apr 2, 2018Class IIZ-2433-2018Under Investigation by firmFollowing pressurization of the devices, damage to the device handle mechanism may occur, accompanied by a loud noise and potential dispersion of plastic fragments and components.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 14 years and passes through 3 companies; a new generation was cleared every 6 months on median.
  • 7 of the 34 ancestors have a recall of any class.
  • Of its descendants, K090872 (Cardica, Inc., 2009) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K053524.

How does its category compare?

All FZP devices

FZP Clip, Implantable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · FZP

5in 2025

2007: 62008: 42009: 32010: 62011: 32012: 22013: 32014: 32015: 82016: 52017: 42018: 42019: 12020: 22022: 32023: 32024: 22025: 52026 (partial year): 2
2007high 8 (2015) · low 0 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FZP

90in 2025

2007: 31 days median2008: 23 days median2009: 22 days median2010: 47 days median2011: 124 days median2013: 47 days median2014: 29 days median2015: 182 days median2016: 72 days median2017: 29 days median2018: 143 days median2022: 227 days median2023: 65 days median2025: 90 days median
2007high 227 (2022) · low 22 (2009)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FZP

1in 2020

2007: 12008: 62010: 12012: 12014: 12016: 22017: 12019: 32020: 1
2007high 6 (2008) · low 0 (2009)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · FZP

1,902in 2025

2007: 1,8772008: 9812009: 2,1602010: 2,3672011: 1,6782012: 1,6772013: 2,3812014: 2,3202015: 2,8712016: 1,8402017: 2,5942018: 2,7182019: 2,9032020: 1,7602021: 1,7592022: 1,5752023: 1,9182024: 2,0672025: 1,902
2007high 2,903 (2019) · low 981 (2008)2025

MAUDE reports naming product code FZP, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200763111,877
20084236981
200932202,160
201064712,367
2011312401,678
20122—11,677
201334702,381
201432912,320
2015818202,871
201657221,840
201742912,594
2018414302,718
20191—32,903
20202—11,760
20210—01,759
2022322701,575
202336501,918
20242—02,067
202559001,902
20262—0—

What is it indicated for?

The Cardica C-Port® xA Anastomosis System is intended for the creation of anastomoses in blood vessels and grafts, including use in coronary artery bypass grafting procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K063644: Cardica C-Port XA Distal Anastomosis System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K063644

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026