510(k) Report

510(k) · Cleared

Cleared

Ussc Braided Synthetic Absorbable Suture

K961997510(k) TraditionalCleared Jul 16, 199655-day reviewClass II21 CFR 878.4493

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

United States Surgical, A Division of Tyco Healthc · GAM Suture, Absorbable, Synthetic, Polyglycolic Acid

Cleared on Jul 16, 1996 after a 55-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 9 later devices descend from it.

Decided
Jul 16, 1996
Review
55 days
Class
Class II
Product code
GAM
Recalls
None
Predicates
0

9 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 1997: 1 descendant cleared1998: 1 descendant cleared2007: 1 descendant cleared2021: 2 descendants cleared2008: 1 descendant cleared2018: 1 descendant cleared2020: 1 descendant cleared2023: 1 descendant cleared1995200020052010201520202025
  1. This deviceK961997 Ussc Braided Synthetic Absorbable SutureUnited States Surgical, A Division of Tyco Healthc · 1996
  2. Descendant · cites it directly · 8 of its ownK970863 Modified Ussc* Polysorb SutureUnited States Surgical, A Division of Tyco Healthc · 1997
  3. Descendant · 2 generations on · 7 of its ownK981935 Polysorb SutureUnited States Surgical, A Division of Tyco Healthc · 1998 · Recalled
  4. Descendant · 3 generations on · 3 of its ownK063536 Polysorb* Synthetic Absorbable Suture with Modified PackagingTyco Healthcare Group · 2007
  5. Descendant · 3 generations on · 2 of its ownK202950 StitchKit COMBOOrigami Surgical · 2021
  6. Descendant · 4 generations on · 2 of its ownK073614 WG-Surgical Sutures with NeedleFoosin Medical Supplies, Inc. · 2008

Showing 5 of 9 descendants. See all descendants

Descendants cleared per year

1997: 11998: 12007: 12008: 12018: 12020: 12021: 22023: 1
1997high 2 (2021) · low 0 (1999)2026

Most influential descendants

Showing 5 of 9 · See all
  • K970863Modified Ussc* Polysorb SutureUnited States Surgical, A Division of Tyco Healthc · 1997 · cites it directly8descendants
  • K981935Polysorb SutureUnited States Surgical, A Division of Tyco Healthc · 1998 · 2 generations on7descendants
  • K063536Polysorb* Synthetic Absorbable Suture with Modified PackagingTyco Healthcare Group · 2007 · 3 generations on3descendants
  • K202950StitchKit COMBOOrigami Surgical · 2021 · 3 generations on2descendants
  • K073614WG-Surgical Sutures with NeedleFoosin Medical Supplies, Inc. · 2008 · 4 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K961997Ussc Braided Synthetic Absorbable SutureUnited States Surgical, A Division of Tyco Healthc1996—
+1K970863Modified Ussc* Polysorb SutureUnited States Surgical, A Division of Tyco Healthc1997—
+2K981935Polysorb SutureUnited States Surgical, A Division of Tyco Healthc19981
+3K063536Polysorb* Synthetic Absorbable Suture with Modified PackagingTyco Healthcare Group2007—
+3K202950StitchKit COMBOOrigami Surgical2021—
+4K073614WG-Surgical Sutures with NeedleFoosin Medical Supplies, Inc.2008—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
199810
200710
200810
201810
202010
202120
202310
FIG. 1 — Lineage of K961997, 1996–2023Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in GAM? 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 GAM device

  1. #1 K252743 STRATAFIX™ Spiral PDS™ Plus Knotless Tissue…score 14.8 · 15 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (9)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K970863Modified Ussc* Polysorb SutureUnited States Surgical, A Division of Tyco Healthc19978

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?

  • Of its descendants, K970863 (United States Surgical, A Division of Tyco Healthc, 1997) has gone furthest, with 8 descendants of its own.

How does its category compare?

All GAM devices

GAM Suture, Absorbable, Synthetic, Polyglycolic Acid: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GAM

3in 2025

2007: 72008: 62009: 32010: 12011: 22012: 52013: 12014: 102015: 52016: 32017: 82018: 52019: 42020: 32021: 22022: 22023: 12024: 22025: 32026 (partial year): 4
2007high 10 (2014) · low 1 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GAM

29in 2025

2007: 50 days median2008: 174 days median2009: 10 days median2012: 31 days median2014: 121 days median2015: 209 days median2016: 169 days median2017: 134 days median2018: 98 days median2019: 90 days median2020: 140 days median2025: 29 days median2026 (partial year): 131 days median
2007high 209 (2015) · low 10 (2009)2026

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

Recalls per year · GAM

1in 2024

2007: 102008: 12009: 62010: 32011: 62016: 12017: 12019: 12020: 442022: 42024: 12026 (partial year): 2
2007high 44 (2020) · low 0 (2012)2026

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

Adverse event reports per year · GAM

8,970in 2025

2007: 2742008: 1942009: 2872010: 5872011: 6372012: 8682013: 8982014: 1,4102015: 9352016: 1,1122017: 1,4992018: 2,2292019: 3,5642020: 3,4152021: 4,5062022: 4,8142023: 5,0702024: 7,2262025: 8,970
2007high 8,970 (2025) · low 194 (2008)2025

MAUDE reports naming product code GAM, 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
200775010274
200861741194
20093106287
20101—3587
20112—6637
20125310868
20131—0898
20141012101,410
201552090935
2016316911,112
2017813411,499
201859802,229
201949013,564
20203140443,415
20212—04,506
20222—44,814
20231—05,070
20242—17,226
202532908,970
202641312—
Cite this page

510(k) Report. “K961997: Ussc Braided Synthetic Absorbable Suture.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K961997

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026