510(k) · Cleared
ClearedQuill Quadrahelix Tissue-Closure Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Angiotech · GAW Suture, Nonabsorbable, Synthetic, Polypropylene
Cleared on Jan 20, 2012 as substantially equivalent to K052373 (Quill Medical, Inc., 2005) after a 28-day review. Its family tree reaches back 7 generations to 2002. 3 later devices descend from it.
- Decided
- Jan 20, 2012
- Review
- 28 days
- Class
- Class II
- Product code
- GAW
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 7 generations to K014153 (2002). 16 ancestors in all, the oldest K915489 (1992). 3 later devices descend from it, 1 citing it directly.
- Root · 7 generations backK014153 Coapt Systmes Endotine DeviceCoapt Systems, Inc. · 2002
- 6 generations backK023922 Coapt Systems Endotine Device, Model CFD-101-00197Coapt Systems, Inc. · 2002
- 5 generations backK032698 Coapt Endotine Midface-ST 4.5 DeviceCoapt Systems, Inc. · 2003
- 4 generations backK041593 Featherlift Extended Length Aptos ThreadSurgical Specialties Corp · 2004
- 3 generations backK050548 Contour Midface Opposing Uni-Directional ThreadsSurgical Specialties Corp · 2005
- 2 generations backK051609 Quill Synthetic Absorbable Barbed SutureQuill Medical, Inc. · 2005
- 1 generation backK052373 Quill Nonabsorbable Polypropylene Barbed SutureQuill Medical, Inc. · 2005
- This deviceK113800 Quill Quadrahelix Tissue-Closure DeviceAngiotech · 2012
- Descendant · cites it directly · 2 of its ownK131224 Sharpoint Polypropylene Surgical Suture, Look Polypropylene Surgical…Surgical Specialties Corp. Dba Angiotech · 2013
- Descendant · 2 generations on · 0 of its ownK233355 Cypris eXact Suturing SystemCypris Medical · 2024
- Descendant · 2 generations on · 0 of its ownK211178 DURAMESH Mesh SutureMsi · 2022
Most influential descendants
Showing 3 of 3 · See all- K131224Sharpoint Polypropylene Surgical Suture, Look Polypropylene Surgical Suture, Quill…Surgical Specialties Corp. Dba Angiotech · 2013 · cites it directly2descendants
- K233355Cypris eXact Suturing SystemCypris Medical · 2024 · 2 generations on0descendants
- K211178DURAMESH Mesh SutureMsi · 2022 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K014153 | Coapt Systmes Endotine Device | Coapt Systems, Inc. | 2002 | — |
| −6 | K023922 | Coapt Systems Endotine Device, Model CFD-101-00197 | Coapt Systems, Inc. | 2002 | — |
| −5 | K032698 | Coapt Endotine Midface-ST 4.5 Device | Coapt Systems, Inc. | 2003 | — |
| −4 | K041593 | Featherlift Extended Length Aptos Thread | Surgical Specialties Corp | 2004 | — |
| −3 | K050548 | Contour Midface Opposing Uni-Directional Threads | Surgical Specialties Corp | 2005 | — |
| −2 | K051609 | Quill Synthetic Absorbable Barbed Suture | Quill Medical, Inc. | 2005 | — |
| −1 | K052373 | Quill Nonabsorbable Polypropylene Barbed Suture | Quill Medical, Inc. | 2005 | — |
| 0 (this device) | K113800 | Quill Quadrahelix Tissue-Closure Device | Angiotech | 2012 | — |
| +1 | K131224 | Sharpoint Polypropylene Surgical Suture, Look Polypropylene Surgical Suture… | Surgical Specialties Corp. Dba Angiotech | 2013 | — |
| +2 | K233355 | Cypris eXact Suturing System | Cypris Medical | 2024 | — |
| +2 | K211178 | DURAMESH Mesh Suture | Msi | 2022 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1992 | 2 | 0 |
| 1996 | 1 | 0 |
| 1997 | 1 | 0 |
| 1998 | 2 | 0 |
| 2002 | 1 | 0 |
| 2003 | 1 | 0 |
| 2004 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 1 | 0 |
| 2022 | 1 | 0 |
| 2024 | 1 | 0 |
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 GAW? 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 GAW device
- #1 K253572 STRATAFIX™ Spiral PRONOVA™ Unidirectional…score 14.4 · 12 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K052373 | Quill Nonabsorbable Polypropylene Barbed SutureSummary page 1…t code, GAW 21 CFR 878.5010 Class Il Legally marketed K052373: QuiliTh Nonabsorbable Polypropylene Barbed devices to which the Suture devi… | 2005 |
What descends from it? (3)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K131224 | Sharpoint Polypropylene Surgical Suture, Look Polypropylene Surgical Suture, Quill… | 2013 | 2 |
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?
- The line of descent spans 10 years and passes through 4 companies; a new generation was cleared every 9 months on median.
- 4 of the 16 ancestors have a recall of any class.
- Of its descendants, K131224 (Surgical Specialties Corp. Dba Angiotech, 2013) has gone furthest, with 2 descendants of its own.
- 5 other devices also cite its predicate K052373.
How does its category compare?
All GAW devicesGAW Suture, Nonabsorbable, Synthetic, Polypropylene: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.
FDA decisions per year · GAW
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · GAW
80in 2018
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GAW
2so far in 2026, the most since 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · GAW
2,545in 2025
MAUDE reports naming product code GAW, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 1 | — | 1 | 73 |
| 2008 | 0 | — | 0 | 75 |
| 2009 | 0 | — | 0 | 71 |
| 2010 | 2 | — | 0 | 85 |
| 2011 | 0 | — | 0 | 84 |
| 2012 | 3 | 86 | 0 | 194 |
| 2013 | 3 | 36 | 0 | 191 |
| 2014 | 2 | — | 0 | 437 |
| 2015 | 3 | 252 | 0 | 422 |
| 2016 | 1 | — | 0 | 440 |
| 2017 | 3 | 145 | 0 | 413 |
| 2018 | 3 | 80 | 0 | 685 |
| 2019 | 1 | — | 0 | 1,803 |
| 2020 | 2 | — | 0 | 1,493 |
| 2021 | 0 | — | 0 | 1,652 |
| 2022 | 2 | — | 0 | 1,563 |
| 2023 | 1 | — | 0 | 1,811 |
| 2024 | 1 | — | 0 | 2,348 |
| 2025 | 0 | — | 0 | 2,545 |
| 2026 | 1 | — | 2 | — |
What is it indicated for?
Quill™ Quadrahelix Knotless Tissue-Closure Device is indicated for soft tissue approximation excluding closure of the epidermis
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K113800 · printed Nov 6, 2026
Cite this page
510(k) Report. “K113800: Quill Quadrahelix Tissue-Closure Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K113800
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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