510(k) Report

510(k) · Cleared

Cleared

Quill Nonabsorbable Polypropylene Barbed Suture

K052373510(k) AbbreviatedCleared Sep 26, 200527-day reviewClass II21 CFR 878.5010

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

Quill Medical, Inc. · GAW Suture, Nonabsorbable, Synthetic, Polypropylene

Cleared on Sep 26, 2005 as substantially equivalent to K050548 (Surgical Specialties Corp, 2005) and 1 other predicate after a 27-day review. Its family tree reaches back 6 generations to 2002. 10 later devices descend from it.

Decided
Sep 26, 2005
Review
27 days
Class
Class II
Product code
GAW
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K014153 (2002). 15 ancestors in all, the oldest K915489 (1992). 10 later devices descend from it, 6 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2004: 1 other ancestor2003: 1 other ancestor1997: 1 other ancestor2002: 1 other ancestor1998: 2 other ancestors1996: 1 other ancestor1992: 2 other ancestors2013: 2 descendants cleared2012: 1 descendant cleared2017: 1 descendant cleared2026: 1 descendant cleared2005: 1 descendant cleared2015: 1 descendant cleared2022: 1 descendant cleared2024: 1 descendant cleared2020: 1 descendant clearedReference device: K904906 · Sharpoint Polypropylene Nonabsorb Surg Sutures Usp · Chathamborough Research Group, Inc. · 1990 · recalledK014153 · Coapt Systmes Endotine Device · Coapt Systems, Inc. · 2002K023922 · Coapt Systems Endotine Device, Model CFD-101-00197 · Coapt Systems, Inc. · 2002K032698 · Coapt Endotine Midface-ST 4.5 Device · Coapt Systems, Inc. · 2003K041593 · Featherlift Extended Length Aptos Thread · Surgical Specialties Corp · 2004×2: 2 generations cleared close together, K050548 (2005), K051609 (2005) 1990200020102020
  1. Root · 6 generations backK014153 Coapt Systmes Endotine DeviceCoapt Systems, Inc. · 2002
  2. 5 generations backK023922 Coapt Systems Endotine Device, Model CFD-101-00197Coapt Systems, Inc. · 2002
  3. 4 generations backK032698 Coapt Endotine Midface-ST 4.5 DeviceCoapt Systems, Inc. · 2003
  4. 3 generations backK041593 Featherlift Extended Length Aptos ThreadSurgical Specialties Corp · 2004
  5. 2 generations backK050548 Contour Midface Opposing Uni-Directional ThreadsSurgical Specialties Corp · 2005
  6. 1 generation backK051609 Quill Synthetic Absorbable Barbed SutureQuill Medical, Inc. · 2005
  7. This deviceK052373 Quill Nonabsorbable Polypropylene Barbed SutureQuill Medical, Inc. · 2005
  8. Descendant · cites it directly · 5 of its ownK130078 Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop…Surgical Specialties Corp. Dba Angiotech · 2013
  9. Descendant · cites it directly · 3 of its ownK113800 Quill Quadrahelix Tissue-Closure DeviceAngiotech · 2012
  10. Descendant · cites it directly · 2 of its ownK131224 Sharpoint Polypropylene Surgical Suture, Look Polypropylene Surgical…Surgical Specialties Corp. Dba Angiotech · 2013
  11. Descendant · cites it directly · 1 of its ownK171039 Assut Filbloc Permanent SuturesAssut Europe S.P.A. · 2017
  12. Descendant · 2 generations on · 1 of its ownK151112 Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop…Angiotech · 2015

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

2005: 12012: 12013: 22015: 12017: 12020: 12022: 12024: 12026: 1
2005high 2 (2013) · low 0 (2006)2026

Most influential descendants

Showing 5 of 10 · See all
  • K130078Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop DesignSurgical Specialties Corp. Dba Angiotech · 2013 · cites it directly5descendants
  • K113800Quill Quadrahelix Tissue-Closure DeviceAngiotech · 2012 · cites it directly3descendants
  • K131224Sharpoint Polypropylene Surgical Suture, Look Polypropylene Surgical Suture, Quill…Surgical Specialties Corp. Dba Angiotech · 2013 · cites it directly2descendants
  • K171039Assut Filbloc Permanent SuturesAssut Europe S.P.A. · 2017 · cites it directly1descendant
  • K151112Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop DesignAngiotech · 2015 · 2 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K014153Coapt Systmes Endotine DeviceCoapt Systems, Inc.2002—
−5K023922Coapt Systems Endotine Device, Model CFD-101-00197Coapt Systems, Inc.2002—
−4K032698Coapt Endotine Midface-ST 4.5 DeviceCoapt Systems, Inc.2003—
−3K041593Featherlift Extended Length Aptos ThreadSurgical Specialties Corp2004—
−2K050548Contour Midface Opposing Uni-Directional ThreadsSurgical Specialties Corp2005—
−1K051609Quill Synthetic Absorbable Barbed SutureQuill Medical, Inc.2005—
0 (this device)K052373Quill Nonabsorbable Polypropylene Barbed SutureQuill Medical, Inc.2005—
+1K130078Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop DesignSurgical Specialties Corp. Dba Angiotech2013—
+1K113800Quill Quadrahelix Tissue-Closure DeviceAngiotech2012—
+1K131224Sharpoint Polypropylene Surgical Suture, Look Polypropylene Surgical Suture…Surgical Specialties Corp. Dba Angiotech2013—
+1K171039Assut Filbloc Permanent SuturesAssut Europe S.P.A.2017—
+2K151112Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop DesignAngiotech2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199220
199610
199710
199820
200210
200310
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
201210
201320
201510
201710
202010
202210
202410
202610
FIG. 1 — Lineage of K052373, 2002–2026Source: 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 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. #1 K253572 STRATAFIX™ Spiral PRONOVA™ Unidirectional…score 14.4 · 12 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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
*K050548Contour Midface Opposing Uni-Directional Threads
Summary page 1
…• For Material / Technological Characteristics: Contour Midface Opposing Unidirectional Threads TM by Surgical Specialties Corp., 510k K050548 * For Indication for Use based on Technological Characteristics: * Quill® Synthetic Absorbable Barbed Sutu…
Surgical Specialties Corp2005—
*K051609Quill Synthetic Absorbable Barbed Suture
Summary page 1
…* For Indication for Use based on Technological Characteristics: * Quill® Synthetic Absorbable Barbed Suture by Quill Medical, Inc., 510k K051609 4. Device Description: The Quill® Nonabsorbable Polypropylene Barbed Suture is a monofilament, flexible threa…
Quill Medical, Inc.2005—
†K904906Sharpoint Polypropylene Nonabsorb Surg Sutures UspChathamborough Research Group, Inc.19901

Also cleared against K050548: 2 other devices →

What descends from it? (10)

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

NumberDeviceApplicantDecidedDescendants
K130078Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop DesignSurgical Specialties Corp. Dba Angiotech20135
K113800Quill Quadrahelix Tissue-Closure DeviceAngiotech20123
K131224Sharpoint Polypropylene Surgical Suture, Look Polypropylene Surgical Suture, Quill…Surgical Specialties Corp. Dba Angiotech20132
K171039Assut Filbloc Permanent SuturesAssut Europe S.P.A.20171
K253572STRATAFIX™ Spiral PRONOVA™ Unidirectional Knotless Tissue Control Device STRATAFIX™…ETHICON, Inc.20260
K052900Quill Nonabsorbable Nylon Barbed SutureQuill Medical, Inc.20050

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 3 years and passes through 3 companies; a new generation was cleared every 9 months on median.
  • 4 of the 15 ancestors have a recall of any class.
  • Of its descendants, K130078 (Surgical Specialties Corp. Dba Angiotech, 2013) has gone furthest, with 5 descendants of its own.
  • 2 other devices also cite its predicate K050548.

How does its category compare?

All GAW devices

GAW Suture, Nonabsorbable, Synthetic, Polypropylene: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GAW

1in 2024

2007: 12010: 22012: 32013: 32014: 22015: 32016: 12017: 32018: 32019: 12020: 22022: 22023: 12024: 12026 (partial year): 1
2007high 3 (2012) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GAW

80in 2018

2012: 86 days median2013: 36 days median2015: 252 days median2017: 145 days median2018: 80 days median
2007high 252 (2015) · low 36 (2013)2026

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

Recalls per year · GAW

2so far in 2026, the most since 2007

2007: 12026 (partial year): 2
2007high 2 (2026) · low 0 (2008)2026

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

Adverse event reports per year · GAW

2,545in 2025

2007: 732008: 752009: 712010: 852011: 842012: 1942013: 1912014: 4372015: 4222016: 4402017: 4132018: 6852019: 1,8032020: 1,4932021: 1,6522022: 1,5632023: 1,8112024: 2,3482025: 2,545
2007high 2,545 (2025) · low 71 (2009)2025

MAUDE reports naming product code GAW, 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
20071—173
20080—075
20090—071
20102—085
20110—084
20123860194
20133360191
20142—0437
201532520422
20161—0440
201731450413
20183800685
20191—01,803
20202—01,493
20210—01,652
20222—01,563
20231—01,811
20241—02,348
20250—02,545
20261—2—

What is it indicated for?

Quill® Nonabsorbable Polypropylene Barbed Sutures are indicated for soft tissue approximation excluding closure of the epidermis.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K052373: Quill Nonabsorbable Polypropylene Barbed Suture.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K052373

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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