510(k) Report

510(k) · Cleared

Cleared

Autobahn Tissue Closure Device and Disposable Cartridge

K042897510(k) TraditionalCleared Nov 19, 200430-day reviewClass II21 CFR 878.4830

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

Ethicon Endo-Surgery, Inc. · GAL Suture, Absorbable, Natural

Cleared on Nov 19, 2004 as substantially equivalent to K011105 (Qrc Consulting, 2001) after a 30-day review. Its family tree reaches back 1 generation to 2001.

Decided
Nov 19, 2004
Review
30 days
Class
Class II
Product code
GAL
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K011105 (2001). No later device cites it as a predicate yet.

K011105 · Suturtek Fastclose Fascia Closure Device · Qrc Consulting · 20012000200220042006
  1. Root · 1 generation backK011105 Suturtek Fastclose Fascia Closure DeviceQrc Consulting · 2001
  2. This deviceK042897 Autobahn Tissue Closure Device and Disposable CartridgeEthicon Endo-Surgery, Inc. · 2004
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K011105Suturtek Fastclose Fascia Closure DeviceQrc Consulting2001—
0 (this device)K042897Autobahn Tissue Closure Device and Disposable CartridgeEthicon Endo-Surgery, Inc.2004—
FIG. 1 — Lineage of K042897, 2001–2004Source: 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.

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  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against? (1)

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
*K011105Suturtek Fastclose Fascia Closure DeviceQrc Consulting2001—

Also cleared against K011105: 3 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Its one ancestor has no recall.
  • 3 other devices also cite its predicate K011105.

How does its category compare?

All GAL devices

GAL Suture, Absorbable, Natural: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GAL

1in 2015

2008: 12015: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GAL

Too few GAL 510(k)s in any year since 2007 to give a median.

Recalls per year · GAL

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

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

Adverse event reports per year · GAL

117in 2025

2007: 132008: 62009: 252010: 572011: 362012: 272013: 322014: 1572015: 1372016: 872017: 1332018: 2462019: 2292020: 1092021: 1202022: 1302023: 1212024: 1612025: 117
2007high 246 (2018) · low 6 (2008)2025

MAUDE reports naming product code GAL, 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
20070—013
20081—06
20090—025
20100—057
20110—036
20120—027
20130—032
20140—0157
20151—0137
20160—087
20170—0133
20180—0246
20190—1229
20200—0109
20210—0120
20220—0130
20230—0121
20240—0161
20250—0117
20260—0—

What is it indicated for?

The AUTOBAHN Tissue Closure Device and Disposable Cartridge is intended for soft tissue approximation and/ or ligation in general surgical procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K042897: Autobahn Tissue Closure Device and Disposable Cartridge.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K042897

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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